Variant report

Variant	nsv3597
Chromosome Location	chr22:32588424-32632724
allele	n/a
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	ARID3A	chr22:32598554-32598592	HepG2	liver:	n/a	n/a
2	BHLHE40	chr22:32603110-32603242	K562	blood:	n/a	n/a
3	CEBPB	chr22:32598562-32598654	HepG2	liver:	n/a	n/a
4	CEBPB	chr22:32615233-32615336	K562	blood:	n/a	chr22:32615258-32615269
5	CEBPB	chr22:32615114-32615334	HepG2	liver:	n/a	chr22:32615258-32615269
6	CHD2	chr22:32602439-32602553	HepG2	liver:	n/a	n/a
7	CHD2	chr22:32600519-32600649	HepG2	liver:	n/a	n/a
8	CHD2	chr22:32598576-32598708	HepG2	liver:	n/a	n/a
9	CREB1	chr22:32600222-32600512	A549	lung:	n/a	n/a
10	CREB1	chr22:32600165-32600599	H1-hESC	embryonic stem cell:	n/a	n/a
11	CREB1	chr22:32598389-32598809	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr22:32598494-32598740	A549	lung:	n/a	n/a
13	CTBP2	chr22:32600303-32601240	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr22:32602557-32602638	MCF-7	breast:	n/a	n/a
15	CTCF	chr22:32603320-32603470	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr22:32598520-32598670	HEK293	kidney:	n/a	chr22:32598585-32598603
17	CTCF	chr22:32603020-32603170	GM12873	blood:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
18	CTCF	chr22:32598500-32598650	HEEpiC	esophagus:	n/a	chr22:32598585-32598603
19	CTCF	chr22:32602960-32603110	HMF	breast:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
20	CTCF	chr22:32603429-32603432	GM10266	blood:	n/a	n/a
21	CTCF	chr22:32602980-32603130	WERI-Rb-1	eye:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
22	CTCF	chr22:32603321-32603426	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr22:32603020-32603170	GM12869	blood:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
24	CTCF	chr22:32602391-32602722	HepG2	liver:	n/a	chr22:32602699-32602707
25	CTCF	chr22:32602480-32602630	Caco-2	colon:	n/a	n/a
26	CTCF	chr22:32598500-32598650	GM12872	blood:	n/a	chr22:32598585-32598603
27	CTCF	chr22:32598580-32598730	HCM	heart:	n/a	chr22:32598585-32598603
28	CTCF	chr22:32603020-32603170	HRPEpiC	eye:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
29	CTCF	chr22:32598500-32598650	RPTEC	kidney:	n/a	chr22:32598585-32598603
30	CTCF	chr22:32602983-32603159	SK-N-SH_RA	brain:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
31	CTCF	chr22:32602925-32603276	MCF-7	breast:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
32	CTCF	chr22:32629400-32629550	BJ	skin:	n/a	n/a
33	CTCF	chr22:32598500-32598650	AG04449	skin:	n/a	chr22:32598585-32598603
34	CTCF	chr22:32598414-32598762	GM12878	blood:	n/a	chr22:32598585-32598603
35	CTCF	chr22:32603327-32603415	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr22:32602899-32603171	T-47D	breast:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
37	CTCF	chr22:32598540-32598690	WERI-Rb-1	eye:	n/a	chr22:32598585-32598603
38	CTCF	chr22:32596740-32596890	MCF-7	breast:	n/a	chr22:32596876-32596884
39	CTCF	chr22:32603000-32603150	GM06990	blood:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
40	CTCF	chr22:32602940-32603223	LNCaP	prostate:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
41	CTCF	chr22:32602961-32603191	HUVEC	blood vessel:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
42	CTCF	chr22:32598520-32598670	AG09319	gingival:	n/a	chr22:32598585-32598603
43	CTCF	chr22:32603220-32603370	GM12873	blood:	n/a	n/a
44	CTCF	chr22:32602500-32602650	GM12866	blood:	n/a	n/a
45	CTCF	chr22:32603220-32603370	GM12867	blood:	n/a	n/a
46	CTCF	chr22:32598520-32598670	NHEK	skin:	n/a	chr22:32598585-32598603
47	CTCF	chr22:32602980-32603130	K562	blood:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
48	CTCF	chr22:32603000-32603150	HCT-116	colon:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
49	CTCF	chr22:32602982-32603185	GM13976	blood:	n/a	chr22:32603055-32603071 chr22:32603049-32603070 chr22:32603061-32603068 chr22:32603054-32603072 chr22:32603056-32603069
50	CTCF	chr22:32598100-32598250	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:32600914-32600964	AoSMC	blood vessel:	n/a
2	chr22:32600722-32600772	AG09309	skin:	n/a
3	chr22:32598681-32598731	LNCaP	prostate:	n/a
4	chr22:32600914-32600964	AoSMC	blood vessel:	n/a
5	chr22:32600722-32600772	AG09309	skin:	n/a
6	chr22:32598681-32598731	LNCaP	prostate:	n/a
7	chr22:32599516-32599566	SKMC	muscle:	n/a
8	chr22:32599613-32599663	PANC-1	pancreas:	n/a
9	chr22:32601101-32601151	U87	brain:	n/a
10	chr22:32601654-32601704	Jurkat	blood:	n/a
11	chr22:32589380-32589430	HAEpiC	amniotic membrane:	n/a
12	chr22:32599648-32599698	U87	brain:	n/a
13	chr22:32599613-32599663	GM12892	blood:	n/a
14	chr22:32599596-32599646	AG09309	skin:	n/a
15	chr22:32599613-32599663	HNPCEpiC	eye:	n/a
16	chr22:32598570-32598620	AG04449	skin:	fetal
17	chr22:32598716-32598766	U87	brain:	n/a
18	chr22:32599516-32599566	NH-A	brain:	n/a
19	chr22:32598716-32598766	HRPEpiC	eye:	n/a
20	chr22:32600914-32600964	HRPEpiC	eye:	n/a
21	chr22:32590246-32590296	PFSK-1	brain:	n/a
22	chr22:32598716-32598766	HCPEpiC	choroid plexus:	n/a
23	chr22:32599613-32599663	SK-N-SH_RA	brain:	n/a
24	chr22:32598570-32598620	LNCaP	prostate:	n/a
25	chr22:32598681-32598731	SK-N-SH_RA	brain:	n/a
26	chr22:32599596-32599646	HAEpiC	amniotic membrane:	n/a
27	chr22:32598570-32598620	GM12878	blood:	n/a
28	chr22:32598716-32598766	Caco-2	colon:	n/a
29	chr22:32600722-32600772	CMK	blood:	n/a
30	chr22:32600722-32600772	HPAEpiC	pulmonary alveolar:	n/a
31	chr22:32598570-32598620	HRCEpiC	kidney:	n/a
32	chr22:32598479-32598529	NHBE	bronchial:	n/a
33	chr22:32599596-32599646	GM12892	blood:	n/a
34	chr22:32598570-32598620	ECC-1	luminal epithelium:	n/a
35	chr22:32601274-32601324	NH-A	brain:	n/a
36	chr22:32600722-32600772	NT2-D1	testis:	n/a
37	chr22:32598479-32598529	A549	lung:	n/a
38	chr22:32589919-32589969	HEEpiC	esophagus:	n/a
39	chr22:32600722-32600772	HAEpiC	amniotic membrane:	n/a
40	chr22:32598479-32598529	SK-N-SH	brain:	n/a
41	chr22:32598479-32598529	IMR90	lung:	fetal
42	chr22:32599613-32599663	NHDF-neo	bronchial:	n/a
43	chr22:32598570-32598620	HL-60	blood:	n/a
44	chr22:32589380-32589430	A549	lung:	n/a
45	chr22:32589380-32589430	U87	brain:	n/a
46	chr22:32589380-32589430	AG04450	lung:	fetal
47	chr22:32589380-32589430	MCF10A-Er-Src	breast:	n/a
48	chr22:32598681-32598731	HNPCEpiC	eye:	n/a
49	chr22:32598479-32598529	HAEpiC	amniotic membrane:	n/a
50	chr22:32599516-32599566	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32590934-32594665..22:32740683-32750950	H1-hESC	embryonic stem cell:	embryo
2	chr22:32586637..32588277-chr22:32602438..32604395,2	K562	blood:
3	chr22:32621030..32623210-chr22:32626100..32627785,2	K562	blood:
4	22:32606395-32607484..22:32868055-32872511	Hela-S3	cervix:
5	chr22:32598041..32599019-chr22:32774399..32775272,3	MCF-7	breast:
6	chr22:32616040..32616656-chr5:127536813..127537603,2	MCF-7	breast:
7	chr22:32600183..32602641-chr22:32605085..32606709,2	MCF-7	breast:
8	22:32606395-32607484..22:33452523-33459358	Hela-S3	cervix:
9	chr22:32601130..32602920-chr22:32660025..32662874,2	MCF-7	breast:
10	22:31936958-31958600..22:32594665-32606395	K562	blood:
11	chr22:32598513..32599181-chr22:32774588..32775254,2	MCF-7	breast:
12	chr22:32596644..32597356-chr22:32662252..32662826,2	MCF-7	breast:
13	chr22:32598096..32598999-chr22:32661829..32662840,5	MCF-7	breast:
14	chr22:32598171..32598996-chr22:32751498..32752149,2	MCF-7	breast:
15	chr22:32537081..32537949-chr22:32602635..32603271,2	MCF-7	breast:
16	chr22:32621030..32623210-chr22:32626100..32627785,2	K562	blood:

Variant related genes	Relation type
ENSG00000242082	TF binding region
IGLCOR22-1	TF binding region
RFPL2	TF binding region
ENSG00000242082	CpG island
IGLCOR22-1	CpG island
RFPL2	CpG island
ENSG00000100225	chromatin interactions
ENSG00000128276	chromatin interactions
ENSG00000128253	chromatin interactions
ENSG00000214093	chromatin interactions
ENSG00000185666	chromatin interactions
ENSG00000242082	chromatin interactions
ENSG00000239674	chromatin interactions

Extended variants
information (count: 1767 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1767 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3959628	chr22:32589401-32589402	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs3986033	chr22:32589417-32589418	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs5998291	chr22:32589418-32589419	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs3959629	chr22:32589427-32589428	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs142885030	chr22:32589428-32589429	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs550460986	chr22:32589919-32589920	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs150896775	chr22:32589920-32589921	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs373599139	chr22:32589926-32589927	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs187123961	chr22:32589937-32589938	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs537919198	chr22:32589967-32589968	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs546077462	chr22:32590264-32590265	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs375726944	chr22:32590267-32590268	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs559350616	chr22:32590279-32590280	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs2413086	chr22:32590960-32590961	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs561825980	chr22:32590986-32590987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs74635419	chr22:32590994-32590995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530781357	chr22:32590995-32590996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552519425	chr22:32590998-32590999	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs3986030	chr22:32591014-32591015	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs3986021	chr22:32591021-32591022	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs144346616	chr22:32591042-32591043	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs3986022	chr22:32591091-32591092	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2413087	chr22:32591093-32591094	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533268197	chr22:32591100-32591101	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs3986023	chr22:32591216-32591217	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs3986024	chr22:32591246-32591247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528275629	chr22:32591253-32591254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189903958	chr22:32591261-32591262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111517685	chr22:32591344-32591345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs3986025	chr22:32591391-32591392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs2413088	chr22:32591394-32591395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546664082	chr22:32591397-32591398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566557477	chr22:32591399-32591400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs67065908	chr22:32591451-32591452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs3986026	chr22:32591468-32591469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2413089	chr22:32591469-32591470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2007455	chr22:32591514-32591515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2007457	chr22:32591515-32591516	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs549695191	chr22:32591535-32591536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547912081	chr22:32591551-32591552	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368492899	chr22:32591586-32591587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs62239003	chr22:32591608-32591609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78845924	chr22:32591610-32591611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538488274	chr22:32591617-32591618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558398742	chr22:32591634-32591635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187904665	chr22:32591645-32591646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147800053	chr22:32591687-32591688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs62239004	chr22:32591688-32591689	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570675003	chr22:32591703-32591704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148864447	chr22:32591734-32591735	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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

Chromatin state (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32591200-32598000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr22:32592600-32592800	Bivalent Enhancer	Fetal Kidney	kidney
3	chr22:32594200-32597000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr22:32595400-32597800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr22:32595400-32598200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr22:32595600-32598400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr22:32595600-32598600	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr22:32596000-32598000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr22:32596000-32598400	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr22:32596200-32598400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr22:32596200-32598800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr22:32596400-32596600	Enhancers	Spleen	Spleen
13	chr22:32596400-32598200	Enhancers	Primary T cells fromperipheralblood	blood
14	chr22:32596400-32598200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr22:32596400-32598400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr22:32596400-32598400	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr22:32596400-32598600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr22:32596600-32596800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr22:32596600-32596800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr22:32596600-32596800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
21	chr22:32596600-32596800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr22:32596600-32597000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr22:32596600-32598200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr22:32596600-32598800	Weak transcription	Spleen	Spleen
25	chr22:32597000-32597800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr22:32597000-32598400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr22:32597000-32598400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr22:32597800-32598200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr22:32597800-32600800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr22:32598000-32598200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
31	chr22:32598000-32598400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
32	chr22:32598000-32598400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
33	chr22:32598000-32598600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr22:32598000-32598600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
35	chr22:32598200-32598400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr22:32598200-32598400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr22:32598200-32598400	Enhancers	Brain Angular Gyrus	brain
38	chr22:32598200-32598400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr22:32598200-32598600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
40	chr22:32598200-32598600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
41	chr22:32598200-32598600	Bivalent Enhancer	Brain Hippocampus Middle	brain
42	chr22:32598200-32598600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
43	chr22:32598200-32598600	Enhancers	A549	lung
44	chr22:32598200-32598800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr22:32598200-32598800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
46	chr22:32598200-32599200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr22:32598200-32599600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr22:32598200-32600000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr22:32598400-32598600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr22:32598400-32598600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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