Variant report

Variant	nsv588886
Chromosome Location	chr22:30836313-30868418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:726)
CpG islands
(count:428)
Chromatin interactive
region (count:44)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30841192-30841835	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:30847501-30847613	K562	blood:	n/a	n/a
3	ATF1	chr22:30837155-30837416	K562	blood:	n/a	n/a
4	ATF1	chr22:30849932-30849974	K562	blood:	n/a	n/a
5	ATF1	chr22:30838387-30838748	K562	blood:	n/a	n/a
6	ATF2	chr22:30838367-30838816	GM12878	blood:	n/a	n/a
7	ATF2	chr22:30838465-30838726	GM12878	blood:	n/a	n/a
8	BACH1	chr22:30840591-30841094	K562	blood:	n/a	n/a
9	BACH1	chr22:30838379-30838432	K562	blood:	n/a	n/a
10	BCL11A	chr22:30838404-30838746	GM12878	blood:	n/a	n/a
11	BCL3	chr22:30840665-30841071	K562	blood:	n/a	n/a
12	BCLAF1	chr22:30840606-30841251	K562	blood:	n/a	n/a
13	BCLAF1	chr22:30840553-30841349	K562	blood:	n/a	n/a
14	BHLHE40	chr22:30838470-30838657	GM12878	blood:	n/a	n/a
15	BRCA1	chr22:30858970-30859293	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr22:30841083-30841426	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr22:30840756-30841268	K562	blood:	n/a	n/a
18	CEBPB	chr22:30850163-30850412	HepG2	liver:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
19	CEBPB	chr22:30849331-30849518	HepG2	liver:	n/a	chr22:30849455-30849466
20	CEBPB	chr22:30841207-30841826	IMR90	lung:	n/a	n/a
21	CEBPB	chr22:30850194-30850450	ECC-1	luminal epithelium:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
22	CEBPB	chr22:30850032-30850486	A549	lung:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
23	CEBPB	chr22:30841212-30841489	A549	lung:	n/a	n/a
24	CEBPB	chr22:30850131-30850512	H1-hESC	embryonic stem cell:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
25	CEBPB	chr22:30841635-30841835	HepG2	liver:	n/a	n/a
26	CEBPB	chr22:30849356-30849471	K562	blood:	n/a	chr22:30849455-30849466
27	CEBPB	chr22:30842929-30843121	HepG2	liver:	n/a	chr22:30843043-30843054
28	CEBPB	chr22:30850157-30850501	IMR90	lung:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
29	CEBPB	chr22:30841162-30841460	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr22:30850138-30850533	K562	blood:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
31	CEBPB	chr22:30850130-30850453	K562	blood:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
32	CEBPB	chr22:30850160-30850496	HepG2	liver:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
33	CEBPB	chr22:30850167-30850479	MCF-7	breast:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
34	CEBPB	chr22:30850155-30850501	A549	lung:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
35	CEBPB	chr22:30838528-30838700	GM12878	blood:	n/a	n/a
36	CEBPB	chr22:30838347-30838776	GM12878	blood:	n/a	n/a
37	CEBPB	chr22:30850178-30850464	A549	lung:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
38	CEBPB	chr22:30850143-30850507	Hela-S3	cervix:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
39	CEBPB	chr22:30850152-30850471	ECC-1	luminal epithelium:	n/a	chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343 chr22:30850334-30850343
40	CEBPD	chr22:30847480-30847857	K562	blood:	n/a	n/a
41	CEBPD	chr22:30840487-30841249	K562	blood:	n/a	n/a
42	CEBPD	chr22:30840570-30841333	K562	blood:	n/a	n/a
43	CEBPD	chr22:30850196-30850483	K562	blood:	n/a	chr22:30850333-30850344 chr22:30850334-30850343
44	CHD2	chr22:30841159-30841515	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr22:30838534-30838626	GM12878	blood:	n/a	n/a
46	CHD2	chr22:30855310-30855318	GM12878	blood:	n/a	n/a
47	CHD2	chr22:30840623-30841257	K562	blood:	n/a	n/a
48	CHD2	chr22:30847521-30847552	K562	blood:	n/a	n/a
49	CTCF	chr22:30841237-30841506	Lung_OC	lung:	n/a	chr22:30841349-30841367
50	CTCF	chr22:30841260-30841410	AoAF	blood vessel:	n/a	chr22:30841349-30841367

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30855332-30855382	SK-N-MC	brain:	n/a
2	chr22:30855332-30855382	SK-N-MC	brain:	n/a
3	chr22:30867673-30867723	MCF10A-Er-Src	breast:	n/a
4	chr22:30868060-30868110	HCM	heart:	n/a
5	chr22:30868060-30868110	SKMC	muscle:	n/a
6	chr22:30868167-30868217	ECC-1	luminal epithelium:	n/a
7	chr22:30855332-30855382	GM12878	blood:	n/a
8	chr22:30868226-30868276	ProgFib	skin:	n/a
9	chr22:30868060-30868110	U87	brain:	n/a
10	chr22:30868060-30868110	HPAEpiC	pulmonary alveolar:	n/a
11	chr22:30867673-30867723	LNCaP	prostate:	n/a
12	chr22:30855332-30855382	Jurkat	blood:	n/a
13	chr22:30855332-30855382	SKMC	muscle:	n/a
14	chr22:30867673-30867723	Caco-2	colon:	n/a
15	chr22:30855332-30855382	HCT-116	colon:	n/a
16	chr22:30868167-30868217	BJ	skin:	n/a
17	chr22:30868167-30868217	H1-hESC	embryonic stem cell:	embryo
18	chr22:30868226-30868276	PrEC	prostate:	n/a
19	chr22:30867939-30867989	SK-N-SH	brain:	n/a
20	chr22:30867939-30867989	HPAEpiC	pulmonary alveolar:	n/a
21	chr22:30868156-30868206	A549	lung:	n/a
22	chr22:30868226-30868276	Caco-2	colon:	n/a
23	chr22:30868226-30868276	A549	lung:	n/a
24	chr22:30868226-30868276	HRE	kidney:	n/a
25	chr22:30855332-30855382	HIPEpiC	eye:	n/a
26	chr22:30868226-30868276	BJ	skin:	n/a
27	chr22:30867673-30867723	HPAEpiC	pulmonary alveolar:	n/a
28	chr22:30867939-30867989	HCM	heart:	n/a
29	chr22:30867939-30867989	AG10803	skin:	n/a
30	chr22:30867673-30867723	HIPEpiC	eye:	n/a
31	chr22:30868167-30868217	U87	brain:	n/a
32	chr22:30868156-30868206	HRE	kidney:	n/a
33	chr22:30867939-30867989	NHBE	bronchial:	n/a
34	chr22:30868060-30868110	CMK	blood:	n/a
35	chr22:30868226-30868276	U87	brain:	n/a
36	chr22:30867939-30867989	PFSK-1	brain:	n/a
37	chr22:30868167-30868217	AG04450	lung:	fetal
38	chr22:30868156-30868206	SKMC	muscle:	n/a
39	chr22:30868156-30868206	AG04450	lung:	fetal
40	chr22:30867939-30867989	SK-N-MC	brain:	n/a
41	chr22:30868060-30868110	GM12891	blood:	n/a
42	chr22:30868156-30868206	PANC-1	pancreas:	n/a
43	chr22:30868167-30868217	HCPEpiC	choroid plexus:	n/a
44	chr22:30868167-30868217	AG10803	skin:	n/a
45	chr22:30868060-30868110	GM12892	blood:	n/a
46	chr22:30855332-30855382	MCF-7	breast:	n/a
47	chr22:30868156-30868206	GM06990	blood:	n/a
48	chr22:30868156-30868206	ECC-1	luminal epithelium:	n/a
49	chr22:30867939-30867989	GM19239	blood:	n/a
50	chr22:30868156-30868206	AG10803	skin:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30853042..30855861-chr22:30857563..30860328,2	MCF-7	breast:
2	chr22:30847099..30849207-chr22:30861572..30863598,2	K562	blood:
3	chr22:30839961..30842016-chr22:30851349..30853503,2	K562	blood:
4	chr22:30840899..30842135-chr22:30881081..30882272,7	MCF-7	breast:
5	chr22:30827529..30829177-chr22:30839737..30842354,2	K562	blood:
6	chr22:30840134..30842525-chr22:30862585..30865175,2	K562	blood:
7	chr22:30856486..30858439-chr22:30860978..30863657,2	K562	blood:
8	chr22:30841133..30842914-chr22:30970572..30973414,2	MCF-7	breast:
9	chr22:30864340..30866153-chr22:30867781..30869639,2	K562	blood:
10	chr22:30855538..30857991-chr22:30868951..30871570,2	MCF-7	breast:
11	chr22:30841508..30843914-chr22:30845452..30847343,2	K562	blood:
12	chr22:30837994..30839939-chr22:30986496..30988737,2	K562	blood:
13	chr22:30840913..30841844-chr22:30952173..30953003,5	MCF-7	breast:
14	chr22:30839545..30842321-chr22:30849222..30852849,3	K562	blood:
15	chr22:30765777..30768205-chr22:30839224..30841289,2	K562	blood:
16	chr22:30781821..30783349-chr22:30839370..30842109,2	K562	blood:
17	chr22:30848250..30850657-chr22:30859446..30861041,2	K562	blood:
18	chr22:30817233..30818848-chr22:30838471..30840689,2	K562	blood:
19	chr22:30818867..30823842-chr22:30836918..30842867,11	K562	blood:
20	chr22:30858198..30860804-chr22:30864892..30866978,2	K562	blood:
21	chr22:30856486..30858439-chr22:30860978..30863657,2	K562	blood:
22	chr22:30841425..30844218-chr22:30849960..30852881,2	MCF-7	breast:
23	chr22:30868050..30870470-chr22:30889261..30891907,2	K562	blood:
24	chr22:30840578..30841753-chr22:30952118..30952876,3	MCF-7	breast:
25	chr22:30860411..30863254-chr22:30868369..30871984,3	K562	blood:
26	chr22:30840134..30842525-chr22:30862585..30865175,2	K562	blood:
27	chr22:30840620..30841156-chr6:26033422..26033988,2	Hela-S3	cervix:
28	chr22:30840805..30841805-chr22:30881139..30882175,5	MCF-7	breast:
29	chr22:30685629..30687266-chr22:30839148..30841021,2	K562	blood:
30	chr22:30821810..30824396-chr22:30842591..30845035,2	K562	blood:
31	chr22:30839961..30842016-chr22:30851349..30853503,2	K562	blood:
32	chr22:30783511..30785819-chr22:30839208..30841180,2	K562	blood:
33	chr22:30841508..30843914-chr22:30845452..30847343,2	K562	blood:
34	chr22:30818699..30820979-chr22:30839778..30841389,2	K562	blood:
35	chr22:30860411..30863254-chr22:30868369..30871984,3	K562	blood:
36	chr22:30848250..30850657-chr22:30859446..30861041,2	K562	blood:
37	chr22:30847099..30849207-chr22:30861572..30863598,2	K562	blood:
38	chr22:30840880..30841579-chr22:31001151..31002176,4	MCF-7	breast:
39	chr22:30821818..30823815-chr22:30836918..30838469,2	K562	blood:
40	chr22:30751221..30752960-chr22:30840327..30842364,3	K562	blood:
41	chr22:30853042..30855861-chr22:30857563..30860328,2	MCF-7	breast:
42	chr22:30841425..30844218-chr22:30849960..30852881,2	MCF-7	breast:
43	chr22:30839710..30841304-chr22:30897619..30899951,2	K562	blood:
44	chr22:30839545..30842321-chr22:30849222..30852849,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTFP1-6	chr22:30867254-30867326	NONHSAT084786
2	lnc-SEC14L3-1	chr22:30847398-30847659	l_2272_chr22:30840785-30847659_testes
3	lnc-SEC14L3-1	chr22:30845842-30845989	l_2272_chr22:30840785-30847659_testes
4	lnc-SEC14L3-1	chr22:30840786-30841070	l_2272_chr22:30840785-30847659_testes

No data

Variant related genes	Relation type
SEC14L3	TF binding region
SEC14L3	CpG island
ENSG00000137259	chromatin interactions
ENSG00000099999	chromatin interactions
ENSG00000100012	chromatin interactions
ENSG00000099995	chromatin interactions
ENSG00000100029	chromatin interactions
ENSG00000272689	chromatin interactions
ENSG00000128242	chromatin interactions
ENSG00000242114	chromatin interactions
ENSG00000187860	chromatin interactions

Extended variants
information (count: 1344 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5753137	chr22:30836313-30836314	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372686649	chr22:30836325-30836326	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs557052797	chr22:30836345-30836346	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs568849147	chr22:30836383-30836384	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs539465922	chr22:30836391-30836392	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs5753138	chr22:30836392-30836393	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs141849519	chr22:30836422-30836423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150634171	chr22:30836448-30836449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368298810	chr22:30836449-30836450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547085219	chr22:30836498-30836499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548369547	chr22:30836533-30836534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186507524	chr22:30836547-30836548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190458938	chr22:30836553-30836554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139782620	chr22:30836638-30836639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183065528	chr22:30836650-30836651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143760454	chr22:30836654-30836655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188226778	chr22:30836658-30836659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs5753139	chr22:30836670-30836671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375192673	chr22:30836708-30836709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192794642	chr22:30836736-30836737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182738537	chr22:30836737-30836738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550498361	chr22:30836741-30836742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568986573	chr22:30836744-30836745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539165443	chr22:30836748-30836749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551419554	chr22:30836749-30836750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187704873	chr22:30836759-30836760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139730583	chr22:30836761-30836762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144484967	chr22:30836800-30836801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374732984	chr22:30836803-30836804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575208763	chr22:30836811-30836812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375563811	chr22:30836832-30836833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561457860	chr22:30836841-30836842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536101485	chr22:30836856-30836857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557284347	chr22:30836857-30836858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575759198	chr22:30836862-30836863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146646176	chr22:30836883-30836884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544648902	chr22:30836896-30836897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34446310	chr22:30836916-30836917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111945203	chr22:30836928-30836929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575133706	chr22:30836994-30836995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564220182	chr22:30837008-30837009	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572936878	chr22:30837046-30837047	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191334871	chr22:30837047-30837048	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs184588373	chr22:30837107-30837108	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs5753140	chr22:30837125-30837126	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560324998	chr22:30837130-30837131	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531980142	chr22:30837142-30837143	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78491563	chr22:30837212-30837213	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529176742	chr22:30837224-30837225	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552174475	chr22:30837227-30837228	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	22522925	CNVD
Autism	22495309	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30824400-30839000	Weak transcription	Hela-S3	cervix
2	chr22:30831800-30841000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr22:30832000-30841600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr22:30832000-30850000	Weak transcription	Right Atrium	heart
5	chr22:30832200-30852400	Weak transcription	Spleen	Spleen
6	chr22:30832600-30837800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr22:30835200-30837200	Weak transcription	K562	blood
8	chr22:30835400-30836600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr22:30835600-30836400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr22:30835600-30836600	Enhancers	NHEK	skin
11	chr22:30835800-30836400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr22:30835800-30836400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr22:30835800-30836400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr22:30835800-30836400	Enhancers	Esophagus	oesophagus
15	chr22:30835800-30836400	Enhancers	HMEC	breast
16	chr22:30836000-30838400	Enhancers	Ovary	ovary
17	chr22:30836200-30836400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr22:30836400-30839000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr22:30836400-30839000	Weak transcription	HMEC	breast
20	chr22:30836400-30839200	Weak transcription	Esophagus	oesophagus
21	chr22:30836400-30840600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr22:30836600-30838400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr22:30837000-30837200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr22:30837000-30837400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
25	chr22:30837000-30837600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr22:30837200-30837400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr22:30837200-30837400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr22:30837200-30839200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr22:30837200-30839600	Enhancers	K562	blood
30	chr22:30837400-30841200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr22:30837600-30838000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr22:30837600-30838000	Enhancers	GM12878-XiMat	blood
33	chr22:30837600-30839000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr22:30837600-30839400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
35	chr22:30837800-30838200	Weak transcription	NHEK	skin
36	chr22:30837800-30838600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr22:30837800-30838800	Enhancers	Primary B cells from peripheral blood	blood
38	chr22:30837800-30839000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
39	chr22:30837800-30839200	Weak transcription	Left Ventricle	heart
40	chr22:30837800-30839400	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr22:30838000-30838800	Flanking Active TSS	GM12878-XiMat	blood
42	chr22:30838000-30839000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr22:30838000-30839000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr22:30838000-30839200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr22:30838000-30839400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr22:30838000-30839400	Enhancers	Osteobl	bone
47	chr22:30838000-30839800	Enhancers	Dnd41	blood
48	chr22:30838200-30838400	Enhancers	NH-A	brain
49	chr22:30838200-30838600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr22:30838200-30839400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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