Variant report

Variant	rs2938632
Chromosome Location	chr1:144534213-144534214
allele	C/T
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:208)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:144533811..144534341-chrX:153625996..153626604,2	Hela-S3	cervix:
2	chr1:144533809..144534431-chr13:50159258..50160240,2	Hela-S3	cervix:
3	chr1:144533723..144534337-chr17:27620660..27621688,3	Hela-S3	cervix:
4	chr1:144533738..144534494-chr17:61818883..61819501,2	HCT-116	colon:
5	chr1:144533785..144534480-chr7:149535088..149535984,2	Hela-S3	cervix:
6	chr1:144533591..144534251-chr22:39915621..39916126,2	Hela-S3	cervix:
7	chr1:144533879..144534865-chr5:77071427..77072208,2	Hela-S3	cervix:
8	chr1:38061052..38061884-chr1:144533650..144534319,2	Hela-S3	cervix:
9	chr1:144533558..144534385-chr14:50778724..50779632,2	Hela-S3	cervix:
10	chr1:144533458..144534448-chr1:149194159..149194696,17	HCT-116	colon:
11	chr1:144533633..144534543-chr10:3826897..3827887,2	Hela-S3	cervix:
12	chr1:144533626..144534443-chr22:40440110..40440823,3	Hela-S3	cervix:
13	chr1:144533823..144534453-chr6:71376836..71377641,2	Hela-S3	cervix:
14	chr1:144532556..144534353-chr1:147805518..147808374,3	K562	blood:
15	chr1:144526974..144536279-chr1:149221211..149226185,98	K562	blood:
16	chr1:144533543..144534245-chr3:186287654..186288161,2	Hela-S3	cervix:
17	chr1:144533721..144534324-chr5:10249075..10250000,2	Hela-S3	cervix:
18	chr1:144533498..144535527-chr14:56140284..56141806,2	K562	blood:
19	chr1:144530771..144535863-chr1:144988447..145007040,21	K562	blood:
20	chr1:144533626..144534268-chr10:74856178..74856917,2	Hela-S3	cervix:
21	chr1:144533798..144534678-chr6:33239455..33240159,2	Hela-S3	cervix:
22	chr1:144533783..144534572-chr19:40931457..40932145,2	HCT-116	colon:
23	chr1:144534120..144534744-chr11:62648041..62648567,2	Hela-S3	cervix:
24	chr1:144533858..144534676-chr5:137800598..137801362,2	HCT-116	colon:
25	chr1:144534046..144534703-chr8:119123617..119124191,2	Hela-S3	cervix:
26	chr1:144533875..144534458-chr16:11835668..11836348,2	Hela-S3	cervix:
27	chr1:144533721..144534707-chr20:1305699..1306434,2	Hela-S3	cervix:
28	chr1:144533877..144534615-chr15:65596654..65597253,2	HCT-116	colon:
29	chr1:144533804..144534642-chrX:77359329..77359942,2	Hela-S3	cervix:
30	chr1:144533699..144534312-chr12:49525254..49525781,2	Hela-S3	cervix:
31	chr1:116915861..116916793-chr1:144533665..144534285,2	Hela-S3	cervix:
32	chr1:45187271..45188987-chr1:144532926..144535604,2	K562	blood:
33	chr1:32671036..32671786-chr1:144533662..144534285,2	HCT-116	colon:
34	chr1:144533848..144534656-chr15:51057553..51058077,2	Hela-S3	cervix:
35	chr1:144533750..144534587-chr6:134495945..134496542,2	Hela-S3	cervix:
36	chr1:144533704..144534341-chr1:167906119..167906857,2	Hela-S3	cervix:
37	chr1:144533645..144534350-chr1:149215075..149215829,2	HCT-116	colon:
38	chr1:144533945..144534883-chr3:133292589..133293471,2	Hela-S3	cervix:
39	chr1:144534120..144534711-chr12:12870119..12870939,2	Hela-S3	cervix:
40	chr1:144533638..144534730-chr2:88315452..88316503,4	Hela-S3	cervix:
41	chr1:144533567..144534586-chr1:184377390..184378390,5	HCT-116	colon:
42	chr1:144534155..144534665-chr1:150551597..150552482,2	Hela-S3	cervix:
43	chr1:144533892..144534669-chr7:65958197..65958873,2	Hela-S3	cervix:
44	chr1:144533670..144534281-chr11:75273793..75274528,2	HCT-116	colon:
45	chr1:51701826..51702360-chr1:144533729..144534245,2	Hela-S3	cervix:
46	chr1:144533606..144534311-chr10:112631501..112632009,2	Hela-S3	cervix:
47	chr1:144534019..144534627-chr19:46010631..46011263,2	Hela-S3	cervix:
48	chr1:144533742..144534250-chr11:62521251..62521855,2	Hela-S3	cervix:
49	chr1:144533696..144534515-chr1:205180497..205181167,2	Hela-S3	cervix:
50	chr1:144534065..144535931-chr1:145036199..145038965,3	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-2	chr1:144534038-144534457	NONHSAT005812

No data

Variant related genes	Relation type
ENSG00000125753	Chromatin interaction
ENSG00000149257	Chromatin interaction
ENSG00000105887	Chromatin interaction
ENSG00000202496	Chromatin interaction
ENSG00000100219	Chromatin interaction
ENSG00000206737	Chromatin interaction
ENSG00000183891	Chromatin interaction
ENSG00000186020	Chromatin interaction
ENSG00000113838	Chromatin interaction
ENSG00000125375	Chromatin interaction
ENSG00000234684	Chromatin interaction
ENSG00000262420	Chromatin interaction
ENSG00000271991	Chromatin interaction
ENSG00000172270	Chromatin interaction
ENSG00000159208	Chromatin interaction
ENSG00000126777	Chromatin interaction
ENSG00000100227	Chromatin interaction
ENSG00000207349	Chromatin interaction
ENSG00000184009	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000138074	Chromatin interaction
ENSG00000259708	Chromatin interaction
ENSG00000250220	Chromatin interaction
ENSG00000245888	Chromatin interaction
ENSG00000091527	Chromatin interaction
ENSG00000120742	Chromatin interaction
ENSG00000140403	Chromatin interaction
ENSG00000171067	Chromatin interaction
ENSG00000174446	Chromatin interaction
ENSG00000122884	Chromatin interaction
ENSG00000232151	Chromatin interaction
ENSG00000207205	Chromatin interaction
ENSG00000180185	Chromatin interaction
ENSG00000184277	Chromatin interaction
ENSG00000185947	Chromatin interaction
ENSG00000123091	Chromatin interaction
ENSG00000124193	Chromatin interaction
ENSG00000258017	Chromatin interaction
ENSG00000116830	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000177666	Chromatin interaction
ENSG00000124198	Chromatin interaction
ENSG00000021776	Chromatin interaction
ENSG00000136144	Chromatin interaction
ENSG00000083838	Chromatin interaction
ENSG00000270141	Chromatin interaction
ENSG00000112305	Chromatin interaction
ENSG00000007968	Chromatin interaction
ENSG00000269501	Chromatin interaction
ENSG00000166439	Chromatin interaction
ENSG00000110925	Chromatin interaction
ENSG00000198231	Chromatin interaction
ENSG00000119912	Chromatin interaction
ENSG00000233527	Chromatin interaction
ENSG00000268172	Chromatin interaction
ENSG00000252656	Chromatin interaction
ENSG00000267751	Chromatin interaction
ENSG00000102144	Chromatin interaction
ENSG00000197019	Chromatin interaction
ENSG00000108256	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000076003	Chromatin interaction
ENSG00000252826	Chromatin interaction
ENSG00000132466	Chromatin interaction
ENSG00000147403	Chromatin interaction
ENSG00000171863	Chromatin interaction
ENSG00000092841	Chromatin interaction
ENSG00000111276	Chromatin interaction
ENSG00000186908	Chromatin interaction
ENSG00000117862	Chromatin interaction
ENSG00000204856	Chromatin interaction
ENSG00000231721	Chromatin interaction
ENSG00000133398	Chromatin interaction
ENSG00000108264	Chromatin interaction
ENSG00000136854	Chromatin interaction
ENSG00000176619	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000125775	Chromatin interaction
ENSG00000230470	Chromatin interaction
ENSG00000203497	Chromatin interaction
ENSG00000134287	Chromatin interaction
ENSG00000185670	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000243452	Chromatin interaction
ENSG00000146963	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000150593	Chromatin interaction
ENSG00000144895	Chromatin interaction
ENSG00000150756	Chromatin interaction
ENSG00000200156	Chromatin interaction
ENSG00000223473	Chromatin interaction
ENSG00000115415	Chromatin interaction
ENSG00000089053	Chromatin interaction
ENSG00000236943	Chromatin interaction
ENSG00000072121	Chromatin interaction
ENSG00000115073	Chromatin interaction
ENSG00000203814	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000272993	Chromatin interaction
ENSG00000092853	Chromatin interaction
ENSG00000138600	Chromatin interaction
ENSG00000202408	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000160194	Chromatin interaction
ENSG00000249492	Chromatin interaction
ENSG00000134717	Chromatin interaction
ENSG00000111231	Chromatin interaction
ENSG00000182872	Chromatin interaction
ENSG00000272822	Chromatin interaction
ENSG00000120738	Chromatin interaction
ENSG00000175061	Chromatin interaction
ENSG00000151881	Chromatin interaction
ENSG00000146063	Chromatin interaction
ENSG00000153094	Chromatin interaction
ENSG00000065970	Chromatin interaction
ENSG00000120306	Chromatin interaction
ENSG00000136451	Chromatin interaction
ENSG00000113441	Chromatin interaction
ENSG00000133059	Chromatin interaction
ENSG00000185825	Chromatin interaction
ENSG00000237310	Chromatin interaction
ENSG00000115963	Chromatin interaction
ENSG00000181991	Chromatin interaction
ENSG00000087510	Chromatin interaction
ENSG00000166441	Chromatin interaction
ENSG00000266173	Chromatin interaction
ENSG00000118515	Chromatin interaction
ENSG00000127483	Chromatin interaction
ENSG00000079999	Chromatin interaction
ENSG00000197622	Chromatin interaction
ENSG00000149925	Chromatin interaction
ENSG00000160051	Chromatin interaction
ENSG00000212456	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000008405	Chromatin interaction
ENSG00000143570	Chromatin interaction
ENSG00000223501	Chromatin interaction
ENSG00000261202	Chromatin interaction
ENSG00000143458	Chromatin interaction
ENSG00000134697	Chromatin interaction
ENSG00000007944	Chromatin interaction
ENSG00000257548	Chromatin interaction
ENSG00000116863	Chromatin interaction
ENSG00000147123	Chromatin interaction
ENSG00000067082	Chromatin interaction
ENSG00000272426	Chromatin interaction
ENSG00000108588	Chromatin interaction
ENSG00000063177	Chromatin interaction
ENSG00000153208	Chromatin interaction
ENSG00000222724	Chromatin interaction
ENSG00000163399	Chromatin interaction
ENSG00000123908	Chromatin interaction
ENSG00000196204	Chromatin interaction
ENSG00000267598	Chromatin interaction
ENSG00000164040	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000207501	Chromatin interaction
ENSG00000169189	Chromatin interaction
ENSG00000160193	Chromatin interaction
ENSG00000170633	Chromatin interaction
ENSG00000128272	Chromatin interaction
ENSG00000143164	Chromatin interaction
ENSG00000138085	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000082269	Chromatin interaction
ENSG00000145996	Chromatin interaction
ENSG00000128463	Chromatin interaction
ENSG00000108511	Chromatin interaction
ENSG00000136159	Chromatin interaction
ENSG00000226446	Chromatin interaction
ENSG00000175581	Chromatin interaction
ENSG00000256982	Chromatin interaction
ENSG00000242663	Chromatin interaction
ENSG00000170852	Chromatin interaction
ENSG00000182197	Chromatin interaction
ENSG00000178104	Chromatin interaction
ENSG00000113580	Chromatin interaction
ENSG00000270103	Chromatin interaction
ENSG00000168003	Chromatin interaction
ENSG00000136143	Chromatin interaction
ENSG00000230832	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000117054	Chromatin interaction
ENSG00000143158	Chromatin interaction
ENSG00000132142	Chromatin interaction
ENSG00000106479	Chromatin interaction
ENSG00000272755	Chromatin interaction
ENSG00000168040	Chromatin interaction
ENSG00000102996	Chromatin interaction
ENSG00000129810	Chromatin interaction
ENSG00000167460	Chromatin interaction
ENSG00000087299	Chromatin interaction
ENSG00000151422	Chromatin interaction
ENSG00000105137	Chromatin interaction
ENSG00000063854	Chromatin interaction
ENSG00000092531	Chromatin interaction
ENSG00000178607	Chromatin interaction
ENSG00000143578	Chromatin interaction
ENSG00000120093	Chromatin interaction
ENSG00000270022	Chromatin interaction
ENSG00000100354	Chromatin interaction
ENSG00000112308	Chromatin interaction
ENSG00000171530	Chromatin interaction
ENSG00000231500	Chromatin interaction
ENSG00000164087	Chromatin interaction
ENSG00000183598	Chromatin interaction
ENSG00000099622	Chromatin interaction
ENSG00000179119	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10737112	0.83[AMR][1000 genomes]
rs12130335	0.91[AMR][1000 genomes]
rs2455992	0.83[AMR][1000 genomes]
rs2655793	0.83[AMR][1000 genomes]
rs2655794	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28663124	0.83[AMR][1000 genomes]
rs2940060	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003583	chr1:144007818-144543442	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
2	nsv1002681	chr1:144007818-144560590	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
3	nsv1012104	chr1:144007818-144682096	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	260 gene(s)	inside rSNPs	diseases
4	nsv1006330	chr1:144007818-144849544	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	262 gene(s)	inside rSNPs	diseases
5	nsv1001989	chr1:144007818-144873327	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
6	nsv997949	chr1:144007818-144876884	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
7	nsv1010670	chr1:144007818-144880405	Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
8	nsv1010163	chr1:144007818-144884322	Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
9	nsv1014985	chr1:144007818-144949963	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
10	nsv1002373	chr1:144013582-144682096	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	258 gene(s)	inside rSNPs	diseases
11	nsv1007748	chr1:144015838-144682096	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	258 gene(s)	inside rSNPs	diseases
12	nsv997876	chr1:144033939-144538748	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
13	nsv524682	chr1:144034888-144617179	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
14	nsv1007246	chr1:144036737-144560590	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
15	nsv1006612	chr1:144050098-144560590	Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
16	esv1828275	chr1:144274482-145098718	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
17	esv2512286	chr1:144321887-144560360	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	251 gene(s)	inside rSNPs	diseases
18	nsv1014641	chr1:144337917-144880405	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
19	nsv998833	chr1:144337917-144885032	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
20	nsv1009682	chr1:144471974-144876884	Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
21	nsv1008142	chr1:144471974-144880405	Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
22	nsv1001693	chr1:144471974-145290292	Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	311 gene(s)	inside rSNPs	diseases
23	nsv831292	chr1:144506093-144613511	Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	248 gene(s)	inside rSNPs	diseases
24	nsv831303	chr1:144523643-144617215	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	248 gene(s)	inside rSNPs	diseases
25	nsv946237	chr1:144533425-144535801	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	246 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144532800-144534400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:144532800-144534600	ZNF genes & repeats	Spleen	Spleen
3	chr1:144532800-144534800	ZNF genes & repeats	Right Atrium	heart
4	chr1:144533000-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
6	chr1:144533200-144534400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr1:144533200-144534400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
8	chr1:144533200-144534400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
9	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
11	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
13	chr1:144533200-144534400	Active TSS	Right Ventricle	heart
14	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
15	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
16	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	NHEK	skin
17	chr1:144533200-144534600	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:144533200-144534600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:144533200-144534600	Flanking Bivalent TSS/Enh	HepG2	liver
20	chr1:144533200-144534600	ZNF genes & repeats	HSMMtube	muscle
21	chr1:144533400-144534400	Active TSS	H9 Cell Line	embryonic stem cell
22	chr1:144533400-144534400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:144533400-144534400	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:144533400-144534400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
25	chr1:144533400-144534400	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
26	chr1:144533400-144534400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr1:144533400-144534400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr1:144533400-144534400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr1:144533400-144534400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:144533400-144534400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:144533400-144534400	Bivalent/Poised TSS	Aorta	Aorta
32	chr1:144533400-144534400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
33	chr1:144533400-144534400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
34	chr1:144533400-144534400	Flanking Bivalent TSS/Enh	Placenta	Placenta
35	chr1:144533400-144534400	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
36	chr1:144533400-144534400	ZNF genes & repeats	Gastric	stomach
37	chr1:144533400-144534400	Flanking Bivalent TSS/Enh	Placenta Amnion	Placenta Amnion
38	chr1:144533400-144534400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
39	chr1:144533400-144534400	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
40	chr1:144533400-144534400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
41	chr1:144533400-144534400	ZNF genes & repeats	NH-A	brain
42	chr1:144533400-144534600	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr1:144533400-144534600	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
44	chr1:144533600-144534400	Active TSS	H1 Cell Line	embryonic stem cell
45	chr1:144533600-144534400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:144533600-144534400	Active TSS	Muscle Satellite Cultured Cells	--
47	chr1:144533600-144534400	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:144533600-144534400	ZNF genes & repeats	Pancreas	Pancrea
49	chr1:144533600-144534400	ZNF genes & repeats	HSMM	muscle
50	chr1:144533600-144534600	Active TSS	HUES48 Cell Line	embryonic stem cell

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