Variant report

Variant	rs11545612
Chromosome Location	chr9:140135784-140135785
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:119)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:72667956..72668530-chr9:140135073..140135812,3	Hela-S3	cervix:
2	chr1:110576808..110577784-chr9:140135245..140136155,2	Hela-S3	cervix:
3	chr12:125549728..125550387-chr9:140135324..140136102,2	NB4	blood:
4	chr6:26027372..26030332-chr9:140134858..140136489,2	K562	blood:
5	chr3:149094727..149095637-chr9:140135617..140136190,2	Hela-S3	cervix:
6	chr10:93169306..93170178-chr9:140135319..140136083,2	Hela-S3	cervix:
7	chr9:139683838..139686879-chr9:140133317..140137174,3	MCF-7	breast:
8	chr9:140133959..140140503-chr9:140188407..140198633,21	K562	blood:
9	chr12:48099496..48100081-chr9:140135445..140136208,2	Hela-S3	cervix:
10	chr17:7475884..7476642-chr9:140135522..140136679,3	Hela-S3	cervix:
11	chr1:153963069..153963678-chr9:140135306..140135841,2	NB4	blood:
12	chr19:10764730..10765644-chr9:140135330..140136079,2	HCT-116	colon:
13	chr9:139940510..139944903-chr9:140133385..140138257,8	K562	blood:
14	chr9:139699446..139701001-chr9:140135080..140137339,2	K562	blood:
15	chr9:140135678..140137635-chr9:140352214..140353821,2	K562	blood:
16	chr12:54718870..54719421-chr9:140135721..140136230,2	Hela-S3	cervix:
17	chr17:33288007..33288620-chr9:140135302..140136004,2	NB4	blood:
18	chr9:139885572..139888217-chr9:140133732..140136326,3	K562	blood:
19	chr9:140005278..140013743-chr9:140133784..140139915,15	K562	blood:
20	chr9:140005266..140013855-chr9:140133577..140138267,15	K562	blood:
21	chr9:139976678..139982959-chr9:140133062..140138076,10	K562	blood:
22	chr7:25019590..25020319-chr9:140135541..140136131,2	Hela-S3	cervix:
23	chr11:17297507..17298318-chr9:140135332..140136049,2	NB4	blood:
24	chr1:153949709..153950496-chr9:140135742..140136312,2	Hela-S3	cervix:
25	chr17:78120586..78121555-chr9:140135508..140136066,2	Hela-S3	cervix:
26	chr17:56736020..56736877-chr9:140135301..140136264,2	MCF-7	breast:
27	chr9:139971489..139973394-chr9:140133950..140136079,2	MCF-7	breast:
28	chr9:139942819..139945702-chr9:140135282..140137884,2	MCF-7	breast:
29	chr1:249132147..249133237-chr9:140135460..140136191,3	Hela-S3	cervix:
30	chr5:56205217..56205961-chr9:140135473..140136142,2	Hela-S3	cervix:
31	chr9:139837701..139840548-chr9:140135499..140137086,2	K562	blood:
32	chr9:139684839..139687692-chr9:140133379..140136351,2	K562	blood:
33	chr22:36924819..36925416-chr9:140135308..140136099,2	Hela-S3	cervix:
34	chr15:41836113..41836929-chr9:140135486..140135990,2	HCT-116	colon:
35	chr9:140031113..140034780-chr9:140133670..140137486,4	K562	blood:
36	chr6:133119275..133120154-chr9:140135256..140136012,2	HCT-116	colon:
37	chr20:62151838..62152595-chr9:140135238..140136497,3	Hela-S3	cervix:
38	chr17:7487133..7487648-chr9:140135549..140136262,2	Hela-S3	cervix:
39	chr7:100026615..100027183-chr9:140135535..140136247,2	Hela-S3	cervix:
40	chr9:139941747..139946969-chr9:140134389..140137858,6	K562	blood:
41	chr5:40679791..40680505-chr9:140135439..140136378,2	Hela-S3	cervix:
42	chr9:140134587..140137137-chr9:140438794..140441158,2	MCF-7	breast:
43	chr9:139947450..139951444-chr9:140134269..140137084,4	MCF-7	breast:
44	chr5:40834912..40835984-chr9:140135474..140136132,3	Hela-S3	cervix:
45	chr2:215674451..215675259-chr9:140135373..140136063,2	NB4	blood:
46	chr1:1446887..1447703-chr9:140135344..140136060,2	Hela-S3	cervix:
47	chr1:149223422..149224948-chr9:140135638..140138435,2	K562	blood:
48	chr9:139740484..139744006-chr9:140134528..140138502,3	MCF-7	breast:
49	chr9:139922316..139924149-chr9:140135106..140137237,2	MCF-7	breast:
50	chr9:140135021..140137503-chr9:140316214..140317833,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000140829	Chromatin interaction
ENSG00000257433	Chromatin interaction
ENSG00000131148	Chromatin interaction
ENSG00000145592	Chromatin interaction
ENSG00000260996	Chromatin interaction
ENSG00000206737	Chromatin interaction
ENSG00000171161	Chromatin interaction
ENSG00000140830	Chromatin interaction
ENSG00000051825	Chromatin interaction
ENSG00000196642	Chromatin interaction
ENSG00000198435	Chromatin interaction
ENSG00000233223	Chromatin interaction
ENSG00000182831	Chromatin interaction
ENSG00000180539	Chromatin interaction
ENSG00000272192	Chromatin interaction
ENSG00000263933	Chromatin interaction
ENSG00000107281	Chromatin interaction
ENSG00000248275	Chromatin interaction
ENSG00000151135	Chromatin interaction
ENSG00000188747	Chromatin interaction
ENSG00000176884	Chromatin interaction
ENSG00000137449	Chromatin interaction
ENSG00000125534	Chromatin interaction
ENSG00000256073	Chromatin interaction
ENSG00000213614	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000176978	Chromatin interaction
ENSG00000161960	Chromatin interaction
ENSG00000205268	Chromatin interaction
ENSG00000068137	Chromatin interaction
ENSG00000174197	Chromatin interaction
ENSG00000260329	Chromatin interaction
ENSG00000177954	Chromatin interaction
ENSG00000129351	Chromatin interaction
ENSG00000107331	Chromatin interaction
ENSG00000127528	Chromatin interaction
ENSG00000132406	Chromatin interaction
ENSG00000107317	Chromatin interaction
ENSG00000261226	Chromatin interaction
ENSG00000103932	Chromatin interaction
ENSG00000130921	Chromatin interaction
ENSG00000229117	Chromatin interaction
ENSG00000233016	Chromatin interaction
ENSG00000197956	Chromatin interaction
ENSG00000224662	Chromatin interaction
ENSG00000272896	Chromatin interaction
ENSG00000183576	Chromatin interaction
ENSG00000054148	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000236933	Chromatin interaction
ENSG00000264395	Chromatin interaction
ENSG00000129255	Chromatin interaction
ENSG00000177239	Chromatin interaction
ENSG00000066044	Chromatin interaction
ENSG00000259605	Chromatin interaction
ENSG00000205018	Chromatin interaction
ENSG00000272654	Chromatin interaction
ENSG00000156508	Chromatin interaction
ENSG00000260339	Chromatin interaction
ENSG00000260342	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000100353	Chromatin interaction
ENSG00000177732	Chromatin interaction
ENSG00000132141	Chromatin interaction
ENSG00000244187	Chromatin interaction
ENSG00000171522	Chromatin interaction
ENSG00000229267	Chromatin interaction
ENSG00000143093	Chromatin interaction
ENSG00000240541	Chromatin interaction
ENSG00000270259	Chromatin interaction
ENSG00000168002	Chromatin interaction
ENSG00000146409	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000148399	Chromatin interaction
ENSG00000198783	Chromatin interaction
ENSG00000176919	Chromatin interaction
ENSG00000237461	Chromatin interaction
ENSG00000141543	Chromatin interaction
ENSG00000100650	Chromatin interaction
ENSG00000186193	Chromatin interaction
ENSG00000187609	Chromatin interaction
ENSG00000070081	Chromatin interaction
ENSG00000173218	Chromatin interaction
ENSG00000238279	Chromatin interaction
ENSG00000128973	Chromatin interaction
ENSG00000182141	Chromatin interaction
ENSG00000222414	Chromatin interaction
ENSG00000225377	Chromatin interaction
ENSG00000260729	Chromatin interaction
ENSG00000081760	Chromatin interaction
ENSG00000148362	Chromatin interaction
ENSG00000155542	Chromatin interaction
ENSG00000143543	Chromatin interaction
ENSG00000124541	Chromatin interaction
ENSG00000159069	Chromatin interaction
ENSG00000268996	Chromatin interaction
ENSG00000108256	Chromatin interaction
ENSG00000230534	Chromatin interaction
ENSG00000111481	Chromatin interaction
ENSG00000197785	Chromatin interaction
ENSG00000264779	Chromatin interaction
ENSG00000143977	Chromatin interaction
ENSG00000070882	Chromatin interaction
ENSG00000188486	Chromatin interaction
ENSG00000184925	Chromatin interaction
ENSG00000005175	Chromatin interaction
ENSG00000143368	Chromatin interaction
ENSG00000213213	Chromatin interaction
ENSG00000177943	Chromatin interaction
ENSG00000054179	Chromatin interaction
ENSG00000165802	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000165338	Chromatin interaction
ENSG00000273066	Chromatin interaction
ENSG00000228544	Chromatin interaction
ENSG00000169908	Chromatin interaction
ENSG00000271576	Chromatin interaction
ENSG00000142207	Chromatin interaction
ENSG00000170540	Chromatin interaction
ENSG00000197355	Chromatin interaction
ENSG00000095794	Chromatin interaction
ENSG00000131143	Chromatin interaction
ENSG00000026025	Chromatin interaction

Extended variants
information (count: 117 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10120415	1.00[EUR][1000 genomes]
rs28548764	1.00[EUR][1000 genomes]
rs28570056	1.00[EUR][1000 genomes]
rs28572030	1.00[EUR][1000 genomes]
rs28589608	1.00[EUR][1000 genomes]
rs28657895	1.00[EUR][1000 genomes]
rs4072322	1.00[EUR][1000 genomes]
rs4073101	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs57870587	1.00[EUR][1000 genomes]
rs58858935	1.00[EUR][1000 genomes]
rs59029792	1.00[EUR][1000 genomes]
rs60184240	1.00[EUR][1000 genomes]
rs61020405	1.00[EUR][1000 genomes]
rs61683906	1.00[EUR][1000 genomes]
rs73565522	1.00[EUR][1000 genomes]
rs73565526	1.00[EUR][1000 genomes]
rs73565528	1.00[EUR][1000 genomes]
rs73565529	1.00[EUR][1000 genomes]
rs7357658	1.00[EUR][1000 genomes]
rs9802728	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv540346	chr9:139360142-140164011	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	471 gene(s)	inside rSNPs	diseases
2	esv2422220	chr9:139478587-140244550	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	454 gene(s)	inside rSNPs	diseases
3	nsv894442	chr9:139544437-140462099	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
4	nsv894452	chr9:139598108-140523429	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
5	nsv894455	chr9:139607966-140411547	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	417 gene(s)	inside rSNPs	diseases
6	nsv894462	chr9:139683224-140274164	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	353 gene(s)	inside rSNPs	diseases
7	nsv894463	chr9:139683224-140411547	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
8	nsv524322	chr9:139690144-140376668	Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	371 gene(s)	inside rSNPs	diseases
9	nsv894470	chr9:139693992-140339091	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	358 gene(s)	inside rSNPs	diseases
10	nsv894474	chr9:139694521-140432318	Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
11	nsv540352	chr9:139695108-140351178	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	358 gene(s)	inside rSNPs	diseases
12	nsv894484	chr9:139709976-140382705	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	360 gene(s)	inside rSNPs	diseases
13	nsv894485	chr9:139709976-140408904	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	363 gene(s)	inside rSNPs	diseases
14	nsv894486	chr9:139725120-140382705	Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	359 gene(s)	inside rSNPs	diseases
15	nsv894487	chr9:139725120-140449582	Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	363 gene(s)	inside rSNPs	diseases
16	esv1803771	chr9:139776400-140274255	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
17	nsv894498	chr9:139810595-140339091	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	324 gene(s)	inside rSNPs	diseases
18	nsv894499	chr9:139810595-140734161	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
19	esv1822764	chr9:139822266-140202692	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	313 gene(s)	inside rSNPs	diseases
20	nsv894501	chr9:139823670-140400275	Genic enhancers Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
21	nsv894502	chr9:139823670-140487108	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
22	esv1823555	chr9:139834714-140362439	Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
23	nsv894506	chr9:139841512-140143801	Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	278 gene(s)	inside rSNPs	diseases
24	nsv894521	chr9:139860631-140228092	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	308 gene(s)	inside rSNPs	diseases
25	nsv894522	chr9:139860631-140411547	Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases
26	nsv894523	chr9:139860631-140462099	Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
27	nsv894553	chr9:139879170-140318758	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	313 gene(s)	inside rSNPs	diseases
28	nsv894554	chr9:139879170-140339091	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	313 gene(s)	inside rSNPs	diseases
29	nsv894556	chr9:139904037-140408904	Active TSS Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
30	nsv894561	chr9:139906359-140143801	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	252 gene(s)	inside rSNPs	diseases
31	nsv894562	chr9:139906359-140382705	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	307 gene(s)	inside rSNPs	diseases
32	nsv894563	chr9:139906359-140408904	Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
33	nsv894564	chr9:139906359-140432318	Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
34	nsv1044451	chr9:139910406-140292556	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
35	nsv894573	chr9:139934020-140218978	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	279 gene(s)	inside rSNPs	diseases
36	nsv894582	chr9:139950351-140218978	Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	276 gene(s)	inside rSNPs	diseases
37	nsv894583	chr9:139950351-140382705	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
38	nsv894584	chr9:139950351-140400275	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	298 gene(s)	inside rSNPs	diseases
39	nsv894586	chr9:139963091-140187734	Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	263 gene(s)	inside rSNPs	diseases
40	nsv894587	chr9:139963091-140291708	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases
41	nsv894588	chr9:139963091-140372570	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	295 gene(s)	inside rSNPs	diseases
42	nsv894590	chr9:139973820-140243547	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	272 gene(s)	inside rSNPs	diseases
43	nsv534403	chr9:139987081-140164480	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	234 gene(s)	inside rSNPs	diseases
44	nsv531601	chr9:139987081-140270240	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	258 gene(s)	inside rSNPs	diseases
45	nsv894592	chr9:139995065-140143801	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	224 gene(s)	inside rSNPs	diseases
46	nsv894594	chr9:139997102-140140871	Genic enhancers Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	222 gene(s)	inside rSNPs	diseases
47	nsv894598	chr9:140003640-140218978	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
48	nsv894603	chr9:140018138-140218978	Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	252 gene(s)	inside rSNPs	diseases
49	nsv894604	chr9:140018138-140233379	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	252 gene(s)	inside rSNPs	diseases
50	nsv894605	chr9:140018138-140291708	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	252 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140133600-140136600	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr9:140133800-140136200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr9:140133800-140136200	Active TSS	NHLF	lung
4	chr9:140133800-140136400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:140133800-140136400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:140133800-140136600	Active TSS	Hela-S3	cervix
7	chr9:140133800-140136600	Active TSS	K562	blood
8	chr9:140133800-140136800	Active TSS	HSMM	muscle
9	chr9:140134000-140136200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:140134000-140136600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr9:140134000-140136600	Active TSS	HepG2	liver
12	chr9:140134200-140136200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:140134200-140136200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr9:140134200-140136200	Active TSS	Muscle Satellite Cultured Cells	--
15	chr9:140134200-140136200	Active TSS	A549	lung
16	chr9:140134200-140136400	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr9:140134200-140136400	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr9:140134200-140136400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr9:140134200-140136400	Active TSS	NHEK	skin
20	chr9:140134200-140136600	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr9:140134200-140136600	Active TSS	H1 Cell Line	embryonic stem cell
22	chr9:140134200-140136600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:140134200-140136600	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr9:140134200-140136600	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr9:140134200-140136600	Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr9:140134200-140136600	Active TSS	Brain Angular Gyrus	brain
27	chr9:140134200-140136600	Active TSS	Brain Anterior Caudate	brain
28	chr9:140134200-140136600	Active TSS	HMEC	breast
29	chr9:140134200-140136600	Active TSS	NHDF-Ad	bronchial
30	chr9:140134200-140136600	Active TSS	Osteobl	bone
31	chr9:140134200-140136800	Active TSS	H9 Cell Line	embryonic stem cell
32	chr9:140134200-140136800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr9:140134200-140137600	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr9:140134400-140136200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr9:140134400-140136200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr9:140134400-140136400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr9:140134400-140136400	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr9:140134400-140136400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:140134400-140136400	Active TSS	Brain Hippocampus Middle	brain
40	chr9:140134400-140136400	Active TSS	Placenta Amnion	Placenta Amnion
41	chr9:140134400-140136400	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr9:140134400-140136400	Active TSS	Right Ventricle	heart
43	chr9:140134400-140136400	Active TSS	Sigmoid Colon	Sigmoid Colon
44	chr9:140134400-140136600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr9:140134400-140136600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr9:140134400-140136600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:140134400-140136600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr9:140134400-140136600	Active TSS	Brain Cingulate Gyrus	brain
49	chr9:140134400-140136600	Active TSS	Fetal Lung	lung
50	chr9:140134400-140136600	Active TSS	Rectal Smooth Muscle	rectum

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