Variant report

Variant	rs9888851
Chromosome Location	chr16:31191372-31191373
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RCOR1	chr16:31189939-31192131	GM12878	blood:	n/a	n/a
2	EP300	chr16:31190996-31192150	HepG2	liver:	n/a	chr16:31191570-31191579
3	ELF1	chr16:31190795-31192249	MCF-7	breast:	n/a	chr16:31191571-31191580 chr16:31191382-31191393 chr16:31191871-31191883
4	GTF2F1	chr16:31190901-31192119	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr16:31190257-31193157	GM12878	blood:	n/a	chr16:31191164-31191174 chr16:31192004-31192013 chr16:31191558-31191568 chr16:31191159-31191169
6	ZKSCAN1	chr16:31190679-31192072	Hela-S3	cervix:	n/a	n/a
7	NANOG	chr16:31191255-31191667	H1-hESC	embryonic stem cell:	n/a	n/a
8	YY1	chr16:31191272-31191872	K562	blood:	n/a	chr16:31191574-31191588 chr16:31191710-31191718 chr16:31191571-31191580 chr16:31191565-31191579 chr16:31191707-31191729 chr16:31191707-31191717 chr16:31191857-31191868 chr16:31191706-31191718
9	GTF2F1	chr16:31190885-31191915	Hela-S3	cervix:	n/a	n/a
10	MAX	chr16:31190500-31192802	HepG2	liver:	n/a	chr16:31192111-31192120 chr16:31190763-31190772
11	POU2F2	chr16:31191239-31192109	GM12878	blood:	n/a	chr16:31191271-31191284 chr16:31191271-31191284 chr16:31191445-31191457
12	PAX5	chr16:31191286-31191613	GM12878	blood:	n/a	n/a
13	MAFF	chr16:31191092-31191540	K562	blood:	n/a	n/a
14	ELF1	chr16:31190941-31191660	HepG2	liver:	n/a	chr16:31191571-31191580 chr16:31191382-31191393
15	CEBPD	chr16:31191246-31192318	K562	blood:	n/a	n/a
16	MAFK	chr16:31190899-31192103	Hela-S3	cervix:	n/a	n/a
17	STAT3	chr16:31191146-31191717	GM12878	blood:	n/a	chr16:31191366-31191374
18	POLR2A	chr16:31190828-31192314	SK-N-MC	brain:	n/a	n/a
19	TAF1	chr16:31190818-31192243	MCF-7	breast:	n/a	n/a
20	ZNF143	chr16:31190717-31192018	K562	blood:	n/a	chr16:31191864-31191882
21	ELF1	chr16:31191081-31192240	MCF-7	breast:	n/a	chr16:31191571-31191580 chr16:31191382-31191393 chr16:31191871-31191883
22	TBP	chr16:31190103-31192399	H1-hESC	embryonic stem cell:	n/a	n/a
23	SIX5	chr16:31191188-31191478	K562	blood:	n/a	n/a
24	JUND	chr16:31190949-31192203	K562	blood:	n/a	chr16:31191742-31191751
25	TAF1	chr16:31191264-31191789	PFSK-1	brain:	n/a	n/a
26	RELA	chr16:31190259-31192150	GM12892	blood:	n/a	n/a
27	RCOR1	chr16:31190619-31192193	Hela-S3	cervix:	n/a	n/a
28	SMC3	chr16:31191266-31192172	K562	blood:	n/a	chr16:31192119-31192129 chr16:31191445-31191455
29	ZNF143	chr16:31190554-31191667	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr16:31190873-31192306	GM12878	blood:	n/a	chr16:31191164-31191174 chr16:31192004-31192013 chr16:31191558-31191568 chr16:31191159-31191169
31	GTF2F1	chr16:31190923-31192232	K562	blood:	n/a	n/a
32	KAT2A	chr16:31191341-31192430	Hela-S3	cervix:	n/a	n/a
33	PBX3	chr16:31191371-31191583	GM12878	blood:	n/a	n/a
34	JUND	chr16:31190149-31192543	GM12878	blood:	n/a	chr16:31191742-31191751
35	MTA3	chr16:31189905-31192315	GM12878	blood:	n/a	n/a
36	SIN3AK20	chr16:31191322-31192212	HepG2	liver:	n/a	n/a
37	MAX	chr16:31190581-31193182	A549	lung:	n/a	chr16:31192111-31192120 chr16:31190763-31190772
38	YY1	chr16:31191272-31192124	HepG2	liver:	n/a	chr16:31191574-31191588 chr16:31191710-31191718 chr16:31191571-31191580 chr16:31191565-31191579 chr16:31191707-31191729 chr16:31191707-31191717 chr16:31191857-31191868 chr16:31191706-31191718
39	MYC	chr16:31190763-31192415	A549	lung:	n/a	chr16:31192111-31192120 chr16:31190763-31190772
40	POLR2A	chr16:31190856-31192293	HEK293	kidney:	n/a	n/a
41	KAT2A	chr16:31191024-31191694	GM12878	blood:	n/a	n/a
42	POLR2A	chr16:31190666-31192976	Hela-S3	cervix:	n/a	n/a
43	STAT5A	chr16:31190839-31192101	GM12878	blood:	n/a	chr16:31191366-31191374
44	HEY1	chr16:31190841-31193110	K562	blood:	n/a	chr16:31191879-31191894 chr16:31191563-31191578 chr16:31191399-31191414 chr16:31191657-31191672 chr16:31191575-31191590
45	POLR2A	chr16:31190895-31193319	K562	blood:	n/a	n/a
46	POLR2A	chr16:31190754-31192802	Hela-S3	cervix:	n/a	n/a
47	HMGN3	chr16:31190738-31192265	K562	blood:	n/a	n/a
48	TAF1	chr16:31190938-31192215	K562	blood:	n/a	n/a
49	SIN3AK20	chr16:31190767-31192780	PANC-1	pancreas:	n/a	n/a
50	E2F4	chr16:31190904-31192678	K562	blood:	n/a	chr16:31191743-31191755 chr16:31191735-31191747 chr16:31191653-31191664 chr16:31191653-31191660 chr16:31192218-31192230 chr16:31191663-31191675 chr16:31191650-31191667 chr16:31191448-31191457 chr16:31192219-31192226 chr16:31191652-31191661 chr16:31191400-31191409 chr16:31191142-31191152 chr16:31192094-31192105 chr16:31192219-31192226 chr16:31191166-31191175 chr16:31192218-31192227 chr16:31192165-31192172 chr16:31192219-31192226 chr16:31191929-31191938 chr16:31191653-31191664 chr16:31191653-31191664 chr16:31192031-31192040

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31191328-31191378	HEK293	kidney:	embryo
2	chr16:31191328-31191378	GM19239	blood:	n/a
3	chr16:31191328-31191378	GM12892	blood:	n/a
4	chr16:31191328-31191378	AG04450	lung:	fetal
5	chr16:31191328-31191378	Caco-2	colon:	n/a
6	chr16:31191328-31191378	MCF-7	breast:	n/a
7	chr16:31191328-31191378	NB4	blood:	n/a
8	chr16:31191328-31191378	HRCEpiC	kidney:	n/a
9	chr16:31191328-31191378	HCT-116	colon:	n/a
10	chr16:31191328-31191378	HIPEpiC	eye:	n/a
11	chr16:31191328-31191378	BJ	skin:	n/a
12	chr16:31191328-31191378	HEEpiC	esophagus:	n/a
13	chr16:31191328-31191378	SAEC	small airway:	n/a
14	chr16:31191328-31191378	HCF	heart:	n/a
15	chr16:31191328-31191378	PFSK-1	brain:	n/a
16	chr16:31191328-31191378	SKMC	muscle:	n/a
17	chr16:31191328-31191378	ECC-1	luminal epithelium:	n/a
18	chr16:31191328-31191378	HUVEC	blood vessel:	n/a
19	chr16:31191328-31191378	SK-N-SH	brain:	n/a
20	chr16:31191328-31191378	LNCaP	prostate:	n/a
21	chr16:31191328-31191378	ovcar-3	ovarian:	n/a
22	chr16:31191328-31191378	U87	brain:	n/a
23	chr16:31191328-31191378	ProgFib	skin:	n/a
24	chr16:31191328-31191378	PANC-1	pancreas:	n/a
25	chr16:31191328-31191378	SK-N-SH_RA	brain:	n/a
26	chr16:31191328-31191378	HCM	heart:	n/a
27	chr16:31191328-31191378	AG10803	skin:	n/a
28	chr16:31191328-31191378	MCF10A-Er-Src	breast:	n/a
29	chr16:31191328-31191378	HepG2	liver:	n/a
30	chr16:31191328-31191378	HCPEpiC	choroid plexus:	n/a
31	chr16:31191328-31191378	NH-A	brain:	n/a
32	chr16:31191328-31191378	RPTEC	kidney:	n/a
33	chr16:31191328-31191378	HAEpiC	amniotic membrane:	n/a
34	chr16:31191328-31191378	IMR90	lung:	fetal
35	chr16:31191328-31191378	A549	lung:	n/a
36	chr16:31191328-31191378	HRPEpiC	eye:	n/a
37	chr16:31191328-31191378	Hepatocyte	liver:	n/a
38	chr16:31191328-31191378	AG04449	skin:	fetal
39	chr16:31191328-31191378	HPAEpiC	pulmonary alveolar:	n/a
40	chr16:31191328-31191378	HL-60	blood:	n/a
41	chr16:31191328-31191378	GM12878	blood:	n/a
42	chr16:31191328-31191378	SK-N-MC	brain:	n/a
43	chr16:31191328-31191378	HMEC	breast:	n/a
44	chr16:31191328-31191378	GM12891	blood:	n/a
45	chr16:31191328-31191378	NHDF-neo	bronchial:	n/a
46	chr16:31191328-31191378	Hela-S3	cervix:	n/a
47	chr16:31191328-31191378	PrEC	prostate:	n/a
48	chr16:31191328-31191378	Jurkat	blood:	n/a
49	chr16:31191328-31191378	CMK	blood:	n/a
50	chr16:31191328-31191378	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:31126778..31130864-chr16:31189092..31195209,17	K562	blood:
2	chr16:31172186..31178618-chr16:31189730..31194059,7	MCF-7	breast:
3	chr16:31189605..31193047-chr16:31225207..31229243,8	MCF-7	breast:
4	chr16:31127491..31131830-chr16:31190393..31192870,6	MCF-7	breast:
5	chr13:49549672..49551500-chr16:31190171..31192875,2	MCF-7	breast:
6	chr1:149858446..149859033-chr16:31191149..31192105,2	Hela-S3	cervix:
7	chr16:31191136..31192870-chr16:31404226..31406023,2	MCF-7	breast:
8	chr16:31191053..31192012-chrX:49041071..49041659,2	Hela-S3	cervix:
9	chr10:60144727..60145603-chr16:31190797..31191683,3	Hela-S3	cervix:
10	chr16:31115614..31117488-chr16:31191253..31194151,3	MCF-7	breast:
11	chr1:86046310..86047174-chr16:31191064..31191786,2	Hela-S3	cervix:
12	chr16:31191300..31192165-chr7:5569505..5570360,3	Hela-S3	cervix:
13	chr16:31190068..31192732-chr16:31364834..31366748,2	MCF-7	breast:
14	chr16:31191222..31191951-chrX:23760549..23761428,2	Hela-S3	cervix:
15	chr16:31190494..31194030-chr16:31469173..31472392,6	MCF-7	breast:
16	chr16:31191197..31191728-chr22:41347161..41348015,2	Hela-S3	cervix:
17	chr16:31098939..31101568-chr16:31190288..31192839,3	MCF-7	breast:
18	chr16:31191033..31191600-chr3:186501235..186501888,2	Hela-S3	cervix:
19	chr16:31184473..31186014-chr16:31191135..31192899,2	MCF-7	breast:
20	chr16:31190876..31193496-chr16:31467915..31469543,2	K562	blood:
21	chr1:110026155..110026667-chr16:31191142..31191720,2	HCT-116	colon:
22	chr16:31189986..31193003-chr16:31453112..31456004,3	MCF-7	breast:
23	chr16:31118660..31120523-chr16:31190662..31192940,2	MCF-7	breast:
24	chr16:31191242..31191910-chr7:139025747..139026482,2	Hela-S3	cervix:
25	chr16:31082536..31087626-chr16:31189682..31193300,10	K562	blood:
26	chr16:31104719..31108663-chr16:31190189..31193568,7	MCF-7	breast:
27	chr16:31190986..31191529-chr20:39945549..39946294,2	Hela-S3	cervix:
28	chr16:31103018..31109714-chr16:31190079..31193155,12	K562	blood:
29	chr11:85358423..85359199-chr16:31191271..31191859,2	Hela-S3	cervix:
30	chr16:31146560..31148604-chr16:31190124..31192018,2	K562	blood:
31	chr16:31190869..31192823-chr20:49543884..49546240,2	MCF-7	breast:
32	chr16:30958732..30963097-chr16:31189619..31195213,8	K562	blood:
33	chr16:31190964..31191933-chr7:148730..149423,2	NB4	blood:
34	chr15:75182375..75183231-chr16:31191121..31191881,2	Hela-S3	cervix:
35	chr16:30708214..30710330-chr16:31190333..31193156,2	K562	blood:
36	chr16:31191033..31191905-chrX:53111335..53111892,2	Hela-S3	cervix:
37	chr16:30886263..30888030-chr16:31191339..31192931,2	K562	blood:
38	chr16:31140279..31143875-chr16:31189793..31193230,5	MCF-7	breast:
39	chr16:31190054..31194646-chr16:31224217..31229118,11	MCF-7	breast:
40	chr16:31191051..31191923-chr7:156685109..156685903,2	Hela-S3	cervix:
41	chr16:30933224..30936181-chr16:31190353..31192929,3	MCF-7	breast:
42	chr16:31191043..31191648-chr19:49375225..49376094,2	NB4	blood:
43	chr16:31117735..31121210-chr16:31190065..31193528,11	K562	blood:
44	chr16:31176133..31177649-chr16:31191065..31192610,2	MCF-7	breast:
45	chr16:31191124..31191940-chr5:95158038..95158783,2	Hela-S3	cervix:
46	chr16:31149707..31163529-chr16:31187237..31198825,44	K562	blood:
47	chr16:31151687..31162079-chr16:31189046..31201898,43	K562	blood:
48	chr16:31189995..31193017-chr16:31468555..31472249,11	K562	blood:
49	chr16:31190260..31192807-chr6:26031049..26033016,2	K562	blood:
50	chr16:31007263..31009136-chr16:31190228..31192701,2	MCF-7	breast:

Variant related genes	Relation type
FUS	TF binding region
FUS	CpG island
ENSG00000236287	Chromatin interaction
ENSG00000174306	Chromatin interaction
ENSG00000175938	Chromatin interaction
ENSG00000102103	Chromatin interaction
ENSG00000102531	Chromatin interaction
ENSG00000120915	Chromatin interaction
ENSG00000152147	Chromatin interaction
ENSG00000184205	Chromatin interaction
ENSG00000162775	Chromatin interaction
ENSG00000261474	Chromatin interaction
ENSG00000151006	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000145012	Chromatin interaction
ENSG00000197451	Chromatin interaction
ENSG00000008294	Chromatin interaction
ENSG00000261385	Chromatin interaction
ENSG00000270066	Chromatin interaction
ENSG00000162650	Chromatin interaction
ENSG00000223247	Chromatin interaction
ENSG00000173457	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000167397	Chromatin interaction
ENSG00000171202	Chromatin interaction
ENSG00000264229	Chromatin interaction
ENSG00000169900	Chromatin interaction
ENSG00000241764	Chromatin interaction
ENSG00000167394	Chromatin interaction
ENSG00000263343	Chromatin interaction
ENSG00000178802	Chromatin interaction
ENSG00000261124	Chromatin interaction
ENSG00000100387	Chromatin interaction
ENSG00000126768	Chromatin interaction
ENSG00000269955	Chromatin interaction
ENSG00000262766	Chromatin interaction
ENSG00000143549	Chromatin interaction
ENSG00000179151	Chromatin interaction
ENSG00000105879	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000103769	Chromatin interaction
ENSG00000112759	Chromatin interaction
ENSG00000164898	Chromatin interaction
ENSG00000115875	Chromatin interaction
ENSG00000006534	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000148444	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000260852	Chromatin interaction
ENSG00000255439	Chromatin interaction
ENSG00000112977	Chromatin interaction
ENSG00000102178	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000052344	Chromatin interaction
ENSG00000262366	Chromatin interaction
ENSG00000140678	Chromatin interaction
ENSG00000225733	Chromatin interaction
ENSG00000113810	Chromatin interaction
ENSG00000129657	Chromatin interaction
ENSG00000075624	Chromatin interaction
ENSG00000012211	Chromatin interaction
ENSG00000116350	Chromatin interaction
ENSG00000197894	Chromatin interaction
ENSG00000175029	Chromatin interaction
ENSG00000265991	Chromatin interaction
ENSG00000197019	Chromatin interaction
ENSG00000136243	Chromatin interaction
ENSG00000104164	Chromatin interaction
ENSG00000177463	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000169896	Chromatin interaction
ENSG00000165752	Chromatin interaction
ENSG00000184009	Chromatin interaction
ENSG00000234912	Chromatin interaction
ENSG00000261487	Chromatin interaction
ENSG00000169223	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000158636	Chromatin interaction
ENSG00000147457	Chromatin interaction
ENSG00000182224	Chromatin interaction
ENSG00000104067	Chromatin interaction
ENSG00000260083	Chromatin interaction
ENSG00000232940	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000123130	Chromatin interaction
ENSG00000142871	Chromatin interaction
ENSG00000101126	Chromatin interaction
ENSG00000137413	Chromatin interaction
ENSG00000242474	Chromatin interaction
ENSG00000255135	Chromatin interaction
ENSG00000167395	Chromatin interaction
ENSG00000107485	Chromatin interaction
ENSG00000056586	Chromatin interaction
ENSG00000103549	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000178226	Chromatin interaction
ENSG00000182718	Chromatin interaction
ENSG00000068885	Chromatin interaction
ENSG00000156886	Chromatin interaction
ENSG00000103507	Chromatin interaction
ENSG00000177238	Chromatin interaction
ENSG00000251131	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000246090	Chromatin interaction
ENSG00000185875	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000184640	Chromatin interaction
ENSG00000260170	Chromatin interaction
ENSG00000163565	Chromatin interaction
ENSG00000183011	Chromatin interaction
ENSG00000252809	Chromatin interaction
ENSG00000108064	Chromatin interaction
ENSG00000074054	Chromatin interaction
ENSG00000180530	Chromatin interaction
ENSG00000101310	Chromatin interaction
ENSG00000096060	Chromatin interaction
ENSG00000173221	Chromatin interaction
ENSG00000112576	Chromatin interaction
ENSG00000176723	Chromatin interaction
ENSG00000156976	Chromatin interaction
ENSG00000070404	Chromatin interaction
ENSG00000028116	Chromatin interaction
ENSG00000139644	Chromatin interaction
ENSG00000181472	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000269897	Chromatin interaction
ENSG00000029363	Chromatin interaction
ENSG00000260911	Chromatin interaction
ENSG00000198113	Chromatin interaction
ENSG00000270959	Chromatin interaction
ENSG00000272324	Chromatin interaction
ENSG00000126217	Chromatin interaction
ENSG00000105983	Chromatin interaction
ENSG00000268863	Chromatin interaction
ENSG00000099365	Chromatin interaction
ENSG00000087074	Chromatin interaction
ENSG00000103496	Chromatin interaction

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

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

rs_ID	r²[population]
rs13331793	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13339393	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28428182	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28637378	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34107331	1.00[AMR][1000 genomes]
rs34259949	1.00[AMR][1000 genomes]
rs34831291	1.00[AMR][1000 genomes]
rs34889904	1.00[AMR][1000 genomes]
rs56196402	1.00[AMR][1000 genomes]
rs59076556	1.00[AMR][1000 genomes]
rs61237574	1.00[AMR][1000 genomes]
rs74015066	1.00[AMR][1000 genomes]
rs74015068	1.00[AMR][1000 genomes]
rs74015069	1.00[AMR][1000 genomes]
rs74015071	1.00[AMR][1000 genomes]
rs74015099	1.00[AMR][1000 genomes]
rs74018303	1.00[AMR][1000 genomes]
rs9922051	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9933960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9940181	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers 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	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong 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	253 gene(s)	inside rSNPs	diseases
9	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
10	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
11	nsv905742	chr16:31102321-31247924	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	188 gene(s)	inside rSNPs	diseases
12	nsv542900	chr16:31137352-31197027	Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 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	chr16:31190000-31193600	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr16:31190000-31193600	Active TSS	H9 Cell Line	embryonic stem cell
3	chr16:31190200-31192200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr16:31190200-31192600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr16:31190200-31192600	Active TSS	NHLF	lung
6	chr16:31190200-31193000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr16:31190200-31193800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr16:31190200-31193800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr16:31190400-31191400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:31190400-31192200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr16:31190400-31192200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
12	chr16:31190400-31192200	Active TSS	Colonic Mucosa	Colon
13	chr16:31190400-31192400	Active TSS	Fetal Intestine Small	intestine
14	chr16:31190400-31192600	Active TSS	Fetal Muscle Trunk	muscle
15	chr16:31190400-31192600	Active TSS	Right Ventricle	heart
16	chr16:31190400-31192800	Active TSS	Fetal Lung	lung
17	chr16:31190400-31193000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr16:31190400-31193400	Active TSS	Psoas Muscle	Psoas
19	chr16:31190400-31193600	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr16:31190400-31193600	Active TSS	Left Ventricle	heart
21	chr16:31190600-31191800	Active TSS	Fetal Heart	heart
22	chr16:31190600-31192200	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr16:31190600-31192200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
24	chr16:31190600-31192400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr16:31190600-31192400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr16:31190600-31192400	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr16:31190600-31192600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr16:31190600-31192600	Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr16:31190600-31192600	Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr16:31190600-31192600	Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr16:31190600-31192600	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr16:31190600-31192600	Active TSS	Colon Smooth Muscle	Colon
33	chr16:31190600-31192600	Active TSS	Pancreas	Pancrea
34	chr16:31190600-31192600	Active TSS	Thymus	Thymus
35	chr16:31190600-31192600	Active TSS	A549	lung
36	chr16:31190600-31192800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr16:31190600-31192800	Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr16:31190600-31192800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr16:31190600-31192800	Active TSS	Primary T killer memory cells from peripheral blood	blood
40	chr16:31190600-31192800	Active TSS	Gastric	stomach
41	chr16:31190600-31192800	Active TSS	Lung	lung
42	chr16:31190600-31192800	Active TSS	Placenta Amnion	Placenta Amnion
43	chr16:31190600-31192800	Active TSS	Sigmoid Colon	Sigmoid Colon
44	chr16:31190600-31192800	Active TSS	Small Intestine	intestine
45	chr16:31190600-31192800	Bivalent/Poised TSS	HepG2	liver
46	chr16:31190600-31193000	Active TSS	Aorta	Aorta
47	chr16:31190600-31193200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr16:31190600-31193200	Active TSS	Esophagus	oesophagus
49	chr16:31190600-31193400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr16:31190600-31193600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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