Variant report

Variant	nsv544679
Chromosome Location	chr22:32379851-32462650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:513)
CpG islands
(count:916)
Chromatin interactive
region (count:46)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr22:32419391-32419583	K562	blood:	n/a	n/a
2	ATF2	chr22:32446622-32447182	GM12878	blood:	n/a	chr22:32446876-32446883
3	ATF2	chr22:32446637-32447091	GM12878	blood:	n/a	chr22:32446876-32446883
4	BACH1	chr22:32446768-32446978	K562	blood:	n/a	chr22:32446808-32446822
5	BACH1	chr22:32446608-32447146	H1-hESC	embryonic stem cell:	n/a	chr22:32446808-32446822
6	BATF	chr22:32420822-32421062	GM12878	blood:	n/a	chr22:32420930-32420941
7	BATF	chr22:32446636-32447044	GM12878	blood:	n/a	n/a
8	BATF	chr22:32446634-32447077	GM12878	blood:	n/a	n/a
9	BCL11A	chr22:32446750-32447046	GM12878	blood:	n/a	chr22:32447013-32447022 chr22:32447015-32447024
10	BCL11A	chr22:32391859-32392030	GM12878	blood:	n/a	n/a
11	BCL11A	chr22:32446739-32447029	GM12878	blood:	n/a	chr22:32447013-32447022 chr22:32447015-32447024
12	BCL3	chr22:32416261-32416480	GM12878	blood:	n/a	chr22:32416347-32416356
13	BCL3	chr22:32426855-32427233	GM12878	blood:	n/a	n/a
14	BCL3	chr22:32446736-32447090	GM12878	blood:	n/a	chr22:32447013-32447022 chr22:32447015-32447024
15	BCL3	chr22:32426848-32427249	GM12878	blood:	n/a	n/a
16	BHLHE40	chr22:32391860-32392106	GM12878	blood:	n/a	n/a
17	CBX3	chr22:32446461-32447627	HCT-116	colon:	n/a	n/a
18	CBX3	chr22:32409988-32410278	HCT-116	colon:	n/a	n/a
19	CEBPB	chr22:32446702-32447383	A549	lung:	n/a	chr22:32446870-32446887
20	CEBPB	chr22:32446620-32447460	Hela-S3	cervix:	n/a	chr22:32446870-32446887
21	CEBPB	chr22:32462396-32462623	HepG2	liver:	n/a	chr22:32462506-32462517 chr22:32462504-32462521
22	CEBPB	chr22:32423803-32424085	IMR90	lung:	n/a	chr22:32423954-32423965
23	CEBPB	chr22:32401539-32401824	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr22:32412262-32412310	IMR90	lung:	n/a	n/a
25	CEBPB	chr22:32432898-32433045	K562	blood:	n/a	n/a
26	CEBPB	chr22:32446683-32447064	MCF-7	breast:	n/a	chr22:32446870-32446887
27	CEBPB	chr22:32446718-32446988	HepG2	liver:	n/a	chr22:32446870-32446887
28	CEBPB	chr22:32446656-32447032	K562	blood:	n/a	chr22:32446870-32446887
29	CEBPB	chr22:32423853-32424032	Hela-S3	cervix:	n/a	chr22:32423954-32423965
30	CEBPB	chr22:32401448-32401801	A549	lung:	n/a	n/a
31	CEBPB	chr22:32446657-32447158	ECC-1	luminal epithelium:	n/a	chr22:32446870-32446887
32	CEBPB	chr22:32412188-32412314	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr22:32423820-32424020	H1-hESC	embryonic stem cell:	n/a	chr22:32423954-32423965
34	CEBPB	chr22:32423804-32424100	K562	blood:	n/a	chr22:32423954-32423965
35	CEBPB	chr22:32446349-32447499	HCT-116	colon:	n/a	chr22:32446870-32446887
36	CEBPB	chr22:32446710-32447087	A549	lung:	n/a	chr22:32446870-32446887
37	CEBPB	chr22:32462454-32462592	H1-hESC	embryonic stem cell:	n/a	chr22:32462506-32462517 chr22:32462504-32462521
38	CEBPB	chr22:32423837-32424070	A549	lung:	n/a	chr22:32423954-32423965
39	CEBPB	chr22:32447139-32447373	K562	blood:	n/a	n/a
40	CEBPB	chr22:32446570-32447087	MCF-7	breast:	n/a	chr22:32446870-32446887
41	CEBPB	chr22:32423804-32424124	HepG2	liver:	n/a	chr22:32423954-32423965
42	CEBPB	chr22:32446582-32447168	A549	lung:	n/a	chr22:32446870-32446887
43	CEBPB	chr22:32416088-32416652	HCT-116	colon:	n/a	n/a
44	CEBPB	chr22:32446745-32447196	H1-hESC	embryonic stem cell:	n/a	chr22:32446870-32446887
45	CEBPB	chr22:32446770-32446890	K562	blood:	n/a	chr22:32446870-32446887
46	CEBPB	chr22:32462062-32462099	IMR90	lung:	n/a	chr22:32462073-32462086 chr22:32462073-32462084
47	CEBPB	chr22:32446462-32447661	HCT-116	colon:	n/a	chr22:32446870-32446887
48	CEBPB	chr22:32446673-32447425	K562	blood:	n/a	chr22:32446870-32446887
49	CEBPB	chr22:32416013-32416642	IMR90	lung:	n/a	n/a
50	CEBPB	chr22:32446655-32447056	IMR90	lung:	n/a	chr22:32446870-32446887

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:32442147-32442197	HEK293	kidney:	embryo
2	chr22:32442147-32442197	HEK293	kidney:	embryo
3	chr22:32435499-32435549	K562	blood:	n/a
4	chr22:32439052-32439102	NHBE	bronchial:	n/a
5	chr22:32439254-32439304	RPTEC	kidney:	n/a
6	chr22:32439391-32439441	U87	brain:	n/a
7	chr22:32435553-32435603	HAEpiC	amniotic membrane:	n/a
8	chr22:32438947-32438997	Hela-S3	cervix:	n/a
9	chr22:32435499-32435549	HCPEpiC	choroid plexus:	n/a
10	chr22:32439052-32439102	NB4	blood:	n/a
11	chr22:32435553-32435603	PFSK-1	brain:	n/a
12	chr22:32435515-32435565	HUVEC	blood vessel:	n/a
13	chr22:32441170-32441220	NT2-D1	testis:	n/a
14	chr22:32438993-32439043	HCF	heart:	n/a
15	chr22:32442147-32442197	HepG2	liver:	n/a
16	chr22:32438993-32439043	U87	brain:	n/a
17	chr22:32439391-32439441	NHBE	bronchial:	n/a
18	chr22:32439254-32439304	LNCaP	prostate:	n/a
19	chr22:32439259-32439309	H1-hESC	embryonic stem cell:	embryo
20	chr22:32439254-32439304	HepG2	liver:	n/a
21	chr22:32439259-32439309	AG04449	skin:	fetal
22	chr22:32435614-32435664	HMEC	breast:	n/a
23	chr22:32438947-32438997	MCF10A-Er-Src	breast:	n/a
24	chr22:32439391-32439441	AG09309	skin:	n/a
25	chr22:32435614-32435664	AG09319	gingival:	n/a
26	chr22:32435614-32435664	AG04449	skin:	fetal
27	chr22:32438947-32438997	HCM	heart:	n/a
28	chr22:32439052-32439102	HPAEpiC	pulmonary alveolar:	n/a
29	chr22:32437574-32437624	HAEpiC	amniotic membrane:	n/a
30	chr22:32439391-32439441	ECC-1	luminal epithelium:	n/a
31	chr22:32435553-32435603	U87	brain:	n/a
32	chr22:32435614-32435664	HCM	heart:	n/a
33	chr22:32435499-32435549	PrEC	prostate:	n/a
34	chr22:32435553-32435603	NHDF-neo	bronchial:	n/a
35	chr22:32439052-32439102	HEEpiC	esophagus:	n/a
36	chr22:32438993-32439043	HPAEpiC	pulmonary alveolar:	n/a
37	chr22:32437574-32437624	RPTEC	kidney:	n/a
38	chr22:32437574-32437624	SKMC	muscle:	n/a
39	chr22:32437865-32437915	PANC-1	pancreas:	n/a
40	chr22:32438993-32439043	HepG2	liver:	n/a
41	chr22:32435499-32435549	Jurkat	blood:	n/a
42	chr22:32435553-32435603	AG04449	skin:	fetal
43	chr22:32435499-32435549	NH-A	brain:	n/a
44	chr22:32437574-32437624	ovcar-3	ovarian:	n/a
45	chr22:32439254-32439304	HCM	heart:	n/a
46	chr22:32437865-32437915	AG04449	skin:	fetal
47	chr22:32439391-32439441	PFSK-1	brain:	n/a
48	chr22:32437865-32437915	PFSK-1	brain:	n/a
49	chr22:32435553-32435603	RPTEC	kidney:	n/a
50	chr22:32439391-32439441	HRCEpiC	kidney:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:32420335..32423179-chr22:32427368..32429696,2	K562	blood:
2	chr22:32413743..32416045-chr22:32472580..32474374,2	MCF-7	breast:
3	22:32012966-32043914..22:32413914-32416530	H1-hESC	embryonic stem cell:	embryo
4	22:32360288-32405313..22:32750950-32761732	K562	blood:
5	chr22:32447097..32450334-chr22:32450975..32454393,3	K562	blood:
6	22:32170492-32188129..22:32446418-32450601	K562	blood:
7	22:32413914-32416530..22:32868055-32872511	K562	blood:
8	chr22:32449818..32451630-chr22:32460465..32462874,2	MCF-7	breast:
9	22:31836635-31847259..22:32409994-32413914	K562	blood:
10	22:32012966-32043914..22:32446418-32450601	H1-hESC	embryonic stem cell:	embryo
11	chr22:32415638..32418353-chr22:32445361..32446986,2	K562	blood:
12	22:32409994-32413914..22:33339333-33353583	Hela-S3	cervix:
13	chr22:32447097..32450334-chr22:32450975..32454393,3	K562	blood:
14	22:32162110-32166713..22:32446418-32450601	H1-hESC	embryonic stem cell:	embryo
15	22:32409994-32413914..22:33452523-33459358	Hela-S3	cervix:
16	22:32360288-32405313..22:32868055-32872511	K562	blood:
17	22:32053085-32061138..22:32461576-32467025	Hela-S3	cervix:
18	chr22:32415638..32418353-chr22:32445361..32446986,2	K562	blood:
19	22:32409994-32413914..22:32764253-32784733	K562	blood:
20	chr22:32438378..32439944-chr22:32477571..32479110,2	MCF-7	breast:
21	chr22:32383908..32385591-chr22:32400658..32402581,2	K562	blood:
22	22:32413914-32416530..22:32764253-32784733	H1-hESC	embryonic stem cell:	embryo
23	chr22:32449818..32451630-chr22:32460465..32462874,2	MCF-7	breast:
24	22:32012966-32043914..22:32360288-32405313	K562	blood:
25	22:32409994-32413914..22:32750950-32761732	Hela-S3	cervix:
26	22:32446418-32450601..22:32764253-32784733	K562	blood:
27	22:32427569-32431306..22:33452523-33459358	Hela-S3	cervix:
28	22:32360288-32405313..22:32764253-32784733	K562	blood:
29	22:32413914-32416530..22:32740683-32750950	H1-hESC	embryonic stem cell:	embryo
30	22:31864703-31891033..22:32446418-32450601	K562	blood:
31	chr22:32383908..32385591-chr22:32400658..32402581,2	K562	blood:
32	22:31961151-31976153..22:32446418-32450601	Hela-S3	cervix:
33	22:32461576-32467025..22:32868055-32872511	Hela-S3	cervix:
34	22:32413914-32416530..22:32477762-32487457	K562	blood:
35	chr22:32386867..32389593-chr22:32389765..32391775,2	MCF-7	breast:
36	22:32360288-32405313..22:32740683-32750950	K562	blood:
37	chr22:32420335..32423179-chr22:32427368..32429696,2	K562	blood:
38	22:32405313-32408742..22:33452523-33459358	Hela-S3	cervix:
39	22:31836635-31847259..22:32461576-32467025	Hela-S3	cervix:
40	chr22:32345809..32348159-chr22:32420362..32422364,2	MCF-7	breast:
41	chr22:32386867..32389593-chr22:32389765..32391775,2	MCF-7	breast:
42	22:32360288-32405313..22:32860159-32865649	K562	blood:
43	22:32416680-32427569..22:32868055-32872511	Hela-S3	cervix:
44	22:32360288-32405313..22:33452523-33459358	H1-hESC	embryonic stem cell:	embryo
45	22:32053085-32061138..22:32446418-32450601	K562	blood:
46	22:32413914-32416530..22:32750950-32761732	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YWHAH-6	chr22:32451598-32451742	ucscGeneNc_uc003anh_2
2	lnc-YWHAH-4	chr22:32445931-32446008	NONHSAT084935
3	lnc-YWHAH-6	chr22:32451000-32451087	ucscGeneNc_uc003anh_2
4	lnc-YWHAH-6	chr22:32453477-32453618	ucscGeneNc_uc003anh_2
5	lnc-YWHAH-4	chr22:32439020-32439403	NONHSAT084935

No data

Variant related genes	Relation type
RN7SL305P	TF binding region
SLC5A1	TF binding region
ENSG00000232346	TF binding region
RN7SL305P	CpG island
SLC5A1	CpG island
ENSG00000232346	CpG island
ENSG00000184708	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000100150	chromatin interactions
ENSG00000100225	chromatin interactions
ENSG00000199248	chromatin interactions
ENSG00000243519	chromatin interactions
ENSG00000241954	chromatin interactions
ENSG00000185666	chromatin interactions
ENSG00000230736	chromatin interactions
ENSG00000232218	chromatin interactions
ENSG00000271093	chromatin interactions
ENSG00000100170	chromatin interactions
ENSG00000205853	chromatin interactions
ENSG00000128276	chromatin interactions
ENSG00000184459	chromatin interactions
ENSG00000241878	chromatin interactions

Extended variants
information (count: 2997 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2997 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185088409	chr22:32379931-32379932	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs79173736	chr22:32379966-32379967	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs189556970	chr22:32379981-32379982	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs554626349	chr22:32379991-32379992	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs574511640	chr22:32380040-32380041	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs543426477	chr22:32380048-32380049	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs557262370	chr22:32380061-32380062	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs73162184	chr22:32380068-32380069	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs545981656	chr22:32380102-32380103	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs73884252	chr22:32380104-32380105	Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528580421	chr22:32380124-32380125	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs77970191	chr22:32380129-32380130	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs4488763	chr22:32380164-32380165	Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs143630025	chr22:32380169-32380170	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs115229784	chr22:32380193-32380194	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs571125543	chr22:32380253-32380254	Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs533415989	chr22:32380267-32380268	Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs547185133	chr22:32380308-32380309	Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs567042149	chr22:32380342-32380343	Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs78758103	chr22:32380465-32380466	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs554739442	chr22:32380470-32380471	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs80342684	chr22:32380494-32380495	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs537090326	chr22:32380547-32380548	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs531628163	chr22:32380593-32380594	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs148092633	chr22:32380601-32380602	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs577077967	chr22:32380618-32380619	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs542162183	chr22:32380669-32380670	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs143895505	chr22:32380696-32380697	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs182534238	chr22:32380707-32380708	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs147280959	chr22:32380709-32380710	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs140893806	chr22:32380736-32380737	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs561889474	chr22:32380746-32380747	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs528031167	chr22:32380753-32380754	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs530863687	chr22:32380774-32380775	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs143259528	chr22:32380798-32380799	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs150901670	chr22:32380800-32380801	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs139387462	chr22:32380835-32380836	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs547004734	chr22:32380893-32380894	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs34891444	chr22:32380898-32380899	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs373221196	chr22:32380913-32380914	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs77418985	chr22:32380919-32380920	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs528608956	chr22:32380955-32380956	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs533552247	chr22:32380959-32380960	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs75386630	chr22:32380975-32380976	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs536707307	chr22:32381042-32381043	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs115093146	chr22:32381081-32381082	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs34960243	chr22:32381086-32381087	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs80171224	chr22:32381128-32381129	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs570324726	chr22:32381160-32381161	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs375772734	chr22:32381170-32381171	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
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
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	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD
Breast cancer	22522925	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32379200-32381400	Enhancers	Fetal Intestine Small	intestine
2	chr22:32379200-32384200	Enhancers	Fetal Intestine Large	intestine
3	chr22:32379800-32380200	Enhancers	Fetal Heart	heart
4	chr22:32379800-32380400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr22:32379800-32380400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr22:32379800-32380400	Enhancers	Duodenum Mucosa	Duodenum
7	chr22:32380400-32383000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr22:32381000-32381200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr22:32381400-32382000	Weak transcription	Fetal Intestine Small	intestine
10	chr22:32382000-32387600	Enhancers	Fetal Intestine Small	intestine
11	chr22:32383000-32383600	Enhancers	Duodenum Mucosa	Duodenum
12	chr22:32383000-32384000	Enhancers	Small Intestine	intestine
13	chr22:32383200-32383600	Enhancers	Pancreas	Pancrea
14	chr22:32383600-32383800	Flanking Active TSS	Duodenum Mucosa	Duodenum
15	chr22:32383800-32384000	Enhancers	HMEC	breast
16	chr22:32383800-32384400	Enhancers	Duodenum Mucosa	Duodenum
17	chr22:32384200-32386000	Weak transcription	Fetal Intestine Large	intestine
18	chr22:32386000-32387400	Enhancers	Duodenum Mucosa	Duodenum
19	chr22:32386000-32387400	Enhancers	Fetal Intestine Large	intestine
20	chr22:32392800-32393000	Enhancers	Fetal Intestine Small	intestine
21	chr22:32393000-32394000	Weak transcription	Fetal Intestine Small	intestine
22	chr22:32394000-32395400	Enhancers	Fetal Intestine Small	intestine
23	chr22:32394200-32395400	Enhancers	Duodenum Mucosa	Duodenum
24	chr22:32394200-32397000	Enhancers	Thymus	Thymus
25	chr22:32394600-32395400	Enhancers	Fetal Intestine Large	intestine
26	chr22:32394600-32395400	Enhancers	Stomach Mucosa	stomach
27	chr22:32394600-32397400	Enhancers	Fetal Thymus	thymus
28	chr22:32395400-32396600	Weak transcription	Fetal Intestine Large	intestine
29	chr22:32395400-32396600	Weak transcription	Fetal Intestine Small	intestine
30	chr22:32395800-32396800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr22:32396200-32396800	Enhancers	Placenta Amnion	Placenta Amnion
32	chr22:32396200-32397400	Enhancers	Placenta	Placenta
33	chr22:32396400-32397000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr22:32396600-32397000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr22:32396600-32397600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr22:32396800-32401200	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr22:32397400-32401200	Weak transcription	Placenta	Placenta
38	chr22:32397600-32400800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr22:32400000-32401000	Weak transcription	Fetal Intestine Large	intestine
40	chr22:32400000-32401000	Weak transcription	Fetal Intestine Small	intestine
41	chr22:32400800-32401000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr22:32401000-32401400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr22:32401000-32402400	Enhancers	Fetal Intestine Large	intestine
44	chr22:32401000-32402600	Enhancers	Fetal Intestine Small	intestine
45	chr22:32401200-32402000	Enhancers	Placenta Amnion	Placenta Amnion
46	chr22:32401200-32402200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr22:32401200-32402200	Enhancers	Placenta	Placenta
48	chr22:32401200-32402200	Enhancers	HMEC	breast
49	chr22:32401400-32401800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr22:32401400-32402000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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