Variant report

Variant	nsv1065893
Chromosome Location	chr22:32400566-32453047
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:915)
Chromatin interactive
region (count:39)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

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	chr22:32446637-32447091	GM12878	blood:	n/a	chr22:32446876-32446883
3	ATF2	chr22:32446622-32447182	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	chr22:32446634-32447077	GM12878	blood:	n/a	n/a
7	BATF	chr22:32420822-32421062	GM12878	blood:	n/a	chr22:32420930-32420941
8	BATF	chr22:32446636-32447044	GM12878	blood:	n/a	n/a
9	BCL11A	chr22:32446750-32447046	GM12878	blood:	n/a	chr22:32447013-32447022 chr22:32447015-32447024
10	BCL11A	chr22:32446739-32447029	GM12878	blood:	n/a	chr22:32447013-32447022 chr22:32447015-32447024
11	BCL3	chr22:32426848-32427249	GM12878	blood:	n/a	n/a
12	BCL3	chr22:32426855-32427233	GM12878	blood:	n/a	n/a
13	BCL3	chr22:32446736-32447090	GM12878	blood:	n/a	chr22:32447013-32447022 chr22:32447015-32447024
14	BCL3	chr22:32416261-32416480	GM12878	blood:	n/a	chr22:32416347-32416356
15	CBX3	chr22:32446461-32447627	HCT-116	colon:	n/a	n/a
16	CBX3	chr22:32409988-32410278	HCT-116	colon:	n/a	n/a
17	CEBPB	chr22:32412262-32412310	IMR90	lung:	n/a	n/a
18	CEBPB	chr22:32446349-32447499	HCT-116	colon:	n/a	chr22:32446870-32446887
19	CEBPB	chr22:32447139-32447373	K562	blood:	n/a	n/a
20	CEBPB	chr22:32423853-32424032	Hela-S3	cervix:	n/a	chr22:32423954-32423965
21	CEBPB	chr22:32446702-32447383	A549	lung:	n/a	chr22:32446870-32446887
22	CEBPB	chr22:32446683-32447064	MCF-7	breast:	n/a	chr22:32446870-32446887
23	CEBPB	chr22:32416013-32416642	IMR90	lung:	n/a	n/a
24	CEBPB	chr22:32446655-32447056	IMR90	lung:	n/a	chr22:32446870-32446887
25	CEBPB	chr22:32423804-32424124	HepG2	liver:	n/a	chr22:32423954-32423965
26	CEBPB	chr22:32446708-32447067	ECC-1	luminal epithelium:	n/a	chr22:32446870-32446887
27	CEBPB	chr22:32423804-32424100	K562	blood:	n/a	chr22:32423954-32423965
28	CEBPB	chr22:32423837-32424070	A549	lung:	n/a	chr22:32423954-32423965
29	CEBPB	chr22:32446770-32446890	K562	blood:	n/a	chr22:32446870-32446887
30	CEBPB	chr22:32401539-32401824	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr22:32412188-32412314	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr22:32423803-32424085	IMR90	lung:	n/a	chr22:32423954-32423965
33	CEBPB	chr22:32446582-32447168	A549	lung:	n/a	chr22:32446870-32446887
34	CEBPB	chr22:32422439-32422501	HepG2	liver:	n/a	n/a
35	CEBPB	chr22:32416088-32416652	HCT-116	colon:	n/a	n/a
36	CEBPB	chr22:32423820-32424020	H1-hESC	embryonic stem cell:	n/a	chr22:32423954-32423965
37	CEBPB	chr22:32446710-32447087	A549	lung:	n/a	chr22:32446870-32446887
38	CEBPB	chr22:32446718-32446988	HepG2	liver:	n/a	chr22:32446870-32446887
39	CEBPB	chr22:32446657-32447158	ECC-1	luminal epithelium:	n/a	chr22:32446870-32446887
40	CEBPB	chr22:32401448-32401801	A549	lung:	n/a	n/a
41	CEBPB	chr22:32446656-32447032	K562	blood:	n/a	chr22:32446870-32446887
42	CEBPB	chr22:32446745-32447196	H1-hESC	embryonic stem cell:	n/a	chr22:32446870-32446887
43	CEBPB	chr22:32446462-32447661	HCT-116	colon:	n/a	chr22:32446870-32446887
44	CEBPB	chr22:32432898-32433045	K562	blood:	n/a	n/a
45	CEBPB	chr22:32446620-32447460	Hela-S3	cervix:	n/a	chr22:32446870-32446887
46	CEBPB	chr22:32446673-32447425	K562	blood:	n/a	chr22:32446870-32446887
47	CEBPB	chr22:32446570-32447087	MCF-7	breast:	n/a	chr22:32446870-32446887
48	CHD2	chr22:32446644-32447095	Hela-S3	cervix:	n/a	n/a
49	CREB1	chr22:32446709-32447071	GM12878	blood:	n/a	n/a
50	CREB1	chr22:32446728-32447127	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:32435499-32435549	HRCEpiC	kidney:	n/a
2	chr22:32439052-32439102	AG04450	lung:	fetal
3	chr22:32439259-32439309	IMR90	lung:	fetal
4	chr22:32437574-32437624	GM19239	blood:	n/a
5	chr22:32438947-32438997	GM12891	blood:	n/a
6	chr22:32437865-32437915	SK-N-MC	brain:	n/a
7	chr22:32435515-32435565	PANC-1	pancreas:	n/a
8	chr22:32435639-32435689	HRCEpiC	kidney:	n/a
9	chr22:32439391-32439441	GM12878	blood:	n/a
10	chr22:32439259-32439309	MCF10A-Er-Src	breast:	n/a
11	chr22:32439052-32439102	HPAEpiC	pulmonary alveolar:	n/a
12	chr22:32439259-32439309	HPAEpiC	pulmonary alveolar:	n/a
13	chr22:32435614-32435664	AG09319	gingival:	n/a
14	chr22:32435499-32435549	NHBE	bronchial:	n/a
15	chr22:32439254-32439304	HAEpiC	amniotic membrane:	n/a
16	chr22:32435639-32435689	PANC-1	pancreas:	n/a
17	chr22:32442147-32442197	NH-A	brain:	n/a
18	chr22:32438947-32438997	AG10803	skin:	n/a
19	chr22:32441170-32441220	HL-60	blood:	n/a
20	chr22:32442147-32442197	HCM	heart:	n/a
21	chr22:32442147-32442197	GM12878	blood:	n/a
22	chr22:32435553-32435603	HNPCEpiC	eye:	n/a
23	chr22:32435553-32435603	SK-N-SH	brain:	n/a
24	chr22:32442147-32442197	SAEC	small airway:	n/a
25	chr22:32435553-32435603	GM12878	blood:	n/a
26	chr22:32439052-32439102	GM12891	blood:	n/a
27	chr22:32439254-32439304	HRCEpiC	kidney:	n/a
28	chr22:32439052-32439102	Jurkat	blood:	n/a
29	chr22:32439254-32439304	SAEC	small airway:	n/a
30	chr22:32438993-32439043	CMK	blood:	n/a
31	chr22:32435515-32435565	HCT-116	colon:	n/a
32	chr22:32437865-32437915	GM06990	blood:	n/a
33	chr22:32437865-32437915	GM12878	blood:	n/a
34	chr22:32439254-32439304	HCT-116	colon:	n/a
35	chr22:32441170-32441220	GM19239	blood:	n/a
36	chr22:32435639-32435689	U87	brain:	n/a
37	chr22:32437865-32437915	Hela-S3	cervix:	n/a
38	chr22:32439052-32439102	HCF	heart:	n/a
39	chr22:32438993-32439043	HNPCEpiC	eye:	n/a
40	chr22:32435499-32435549	SK-N-MC	brain:	n/a
41	chr22:32438947-32438997	BE2_C	brain:	n/a
42	chr22:32439391-32439441	MCF-7	breast:	n/a
43	chr22:32435639-32435689	GM19239	blood:	n/a
44	chr22:32439391-32439441	ProgFib	skin:	n/a
45	chr22:32435553-32435603	H1-hESC	embryonic stem cell:	embryo
46	chr22:32435553-32435603	AG04450	lung:	fetal
47	chr22:32435614-32435664	NHDF-neo	bronchial:	n/a
48	chr22:32437574-32437624	NT2-D1	testis:	n/a
49	chr22:32439254-32439304	K562	blood:	n/a
50	chr22:32438993-32439043	AG09309	skin:	n/a

(count:39 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 1844 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1844 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62240621	chr22:32400570-32400571	Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117629537	chr22:32400579-32400580	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs185121093	chr22:32400595-32400596	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs7285190	chr22:32400709-32400710	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs9621376	chr22:32400724-32400725	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs117017176	chr22:32400725-32400726	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs145351339	chr22:32400773-32400774	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs528037264	chr22:32400800-32400801	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs548085210	chr22:32400805-32400806	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs189878219	chr22:32400821-32400822	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs536889008	chr22:32400824-32400825	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs550343827	chr22:32400838-32400839	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs570637332	chr22:32400851-32400852	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs539941902	chr22:32400882-32400883	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs553154544	chr22:32400965-32400966	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs182200998	chr22:32400966-32400967	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs117305417	chr22:32400975-32400976	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs35869862	chr22:32400985-32400986	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs374669703	chr22:32400999-32401000	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs200326348	chr22:32401026-32401027	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs574805011	chr22:32401061-32401062	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs74918002	chr22:32401108-32401109	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs188894538	chr22:32401119-32401120	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs544848782	chr22:32401162-32401163	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs564693117	chr22:32401172-32401173	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs201810095	chr22:32401182-32401183	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs193240845	chr22:32401183-32401184	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs545892306	chr22:32401283-32401284	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs531591483	chr22:32401303-32401304	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs17682583	chr22:32401495-32401496	Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs5749348	chr22:32401532-32401533	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs547774810	chr22:32401534-32401535	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs561679911	chr22:32401542-32401543	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs530692226	chr22:32401565-32401566	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs183516588	chr22:32401588-32401589	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs55788758	chr22:32401635-32401636	Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs539218257	chr22:32401646-32401647	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs547074276	chr22:32401716-32401717	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs188538928	chr22:32401799-32401800	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs149210346	chr22:32401830-32401831	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs191781956	chr22:32401840-32401841	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs73407905	chr22:32401949-32401950	Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538554949	chr22:32401953-32401954	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs77324143	chr22:32401957-32401958	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs532738307	chr22:32401969-32401970	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs183999584	chr22:32402029-32402030	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs188631731	chr22:32402201-32402202	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs559440909	chr22:32402202-32402203	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs552538381	chr22:32402234-32402235	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs371317169	chr22:32402277-32402278	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Acute myeloid leukemia	20729466	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

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32396800-32401200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr22:32397400-32401200	Weak transcription	Placenta	Placenta
3	chr22:32397600-32400800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr22:32400000-32401000	Weak transcription	Fetal Intestine Large	intestine
5	chr22:32400000-32401000	Weak transcription	Fetal Intestine Small	intestine
6	chr22:32400800-32401000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr22:32401000-32401400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr22:32401000-32402400	Enhancers	Fetal Intestine Large	intestine
9	chr22:32401000-32402600	Enhancers	Fetal Intestine Small	intestine
10	chr22:32401200-32402000	Enhancers	Placenta Amnion	Placenta Amnion
11	chr22:32401200-32402200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr22:32401200-32402200	Enhancers	Placenta	Placenta
13	chr22:32401200-32402200	Enhancers	HMEC	breast
14	chr22:32401400-32401800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr22:32401400-32402000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr22:32401400-32402000	Enhancers	Stomach Mucosa	stomach
17	chr22:32401400-32402200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr22:32401400-32402200	Enhancers	Duodenum Mucosa	Duodenum
19	chr22:32409400-32410000	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
20	chr22:32413600-32414600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr22:32413600-32414600	Enhancers	HMEC	breast
22	chr22:32414200-32414400	Enhancers	Osteobl	bone
23	chr22:32414400-32414600	Enhancers	NH-A	brain
24	chr22:32414600-32415800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr22:32414600-32415800	Weak transcription	HMEC	breast
26	chr22:32414600-32415800	Weak transcription	Osteobl	bone
27	chr22:32414600-32416000	Weak transcription	NH-A	brain
28	chr22:32415600-32417000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr22:32415800-32416800	Enhancers	NHEK	skin
30	chr22:32415800-32416800	Enhancers	Osteobl	bone
31	chr22:32415800-32417000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr22:32415800-32417000	Enhancers	HMEC	breast
33	chr22:32416000-32416600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr22:32416000-32416600	Enhancers	HUVEC	blood vessel
35	chr22:32416000-32416800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr22:32416000-32416800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr22:32416000-32416800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr22:32416000-32416800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr22:32416000-32416800	Enhancers	HSMMtube	muscle
40	chr22:32416000-32416800	Enhancers	NH-A	brain
41	chr22:32416000-32417000	Enhancers	HSMM	muscle
42	chr22:32416000-32422200	Enhancers	Fetal Intestine Large	intestine
43	chr22:32416000-32422800	Enhancers	Fetal Intestine Small	intestine
44	chr22:32416200-32416600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr22:32416200-32416600	Enhancers	NHDF-Ad	bronchial
46	chr22:32416400-32416800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr22:32416600-32417000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr22:32416800-32419200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr22:32417000-32417400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr22:32417000-32419200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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