Variant report

Variant	esv1816838
Chromosome Location	chr20:1230185-1247015
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:488)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:1245941-1246879	K562	blood:	n/a	n/a
2	ARID3A	chr20:1234832-1235324	K562	blood:	n/a	n/a
3	ARID3A	chr20:1236287-1236743	K562	blood:	n/a	n/a
4	ATF1	chr20:1244491-1244796	K562	blood:	n/a	n/a
5	ATF1	chr20:1236319-1236702	K562	blood:	n/a	n/a
6	ATF1	chr20:1233040-1233398	K562	blood:	n/a	n/a
7	ATF1	chr20:1245848-1246301	K562	blood:	n/a	n/a
8	ATF3	chr20:1236303-1236655	K562	blood:	n/a	n/a
9	BACH1	chr20:1236391-1236762	K562	blood:	n/a	n/a
10	BHLHE40	chr20:1245962-1246234	K562	blood:	n/a	n/a
11	BHLHE40	chr20:1246620-1246857	K562	blood:	n/a	n/a
12	CBX3	chr20:1236341-1236739	K562	blood:	n/a	n/a
13	CBX3	chr20:1237537-1237935	K562	blood:	n/a	n/a
14	CBX3	chr20:1246477-1247008	K562	blood:	n/a	n/a
15	CBX3	chr20:1236197-1236747	K562	blood:	n/a	n/a
16	CBX3	chr20:1233125-1233387	K562	blood:	n/a	n/a
17	CCNT2	chr20:1245783-1246365	K562	blood:	n/a	n/a
18	CCNT2	chr20:1246607-1247644	K562	blood:	n/a	chr20:1246918-1246927 chr20:1247118-1247127 chr20:1247123-1247132
19	CCNT2	chr20:1234963-1235273	K562	blood:	n/a	n/a
20	CCNT2	chr20:1236340-1236746	K562	blood:	n/a	n/a
21	CEBPB	chr20:1236345-1236668	K562	blood:	n/a	n/a
22	CEBPB	chr20:1236328-1236665	K562	blood:	n/a	n/a
23	CEBPD	chr20:1236273-1236766	K562	blood:	n/a	n/a
24	CEBPD	chr20:1236295-1236780	K562	blood:	n/a	n/a
25	CREB1	chr20:1246671-1246997	A549	lung:	n/a	n/a
26	CREB1	chr20:1246541-1247155	A549	lung:	n/a	n/a
27	CTCF	chr20:1246860-1247010	SK-N-SH_RA	brain:	n/a	chr20:1246967-1246980
28	CTCF	chr20:1246940-1247090	Caco-2	colon:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
29	CTCF	chr20:1246920-1247070	SK-N-SH_RA	brain:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
30	CTCF	chr20:1246955-1247036	GM12878	blood:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
31	CTCF	chr20:1246920-1247070	HepG2	liver:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
32	CTCF	chr20:1246920-1247070	AoAF	blood vessel:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
33	CTCF	chr20:1239302-1239333	Medullo	brain:	n/a	n/a
34	CTCF	chr20:1246840-1246990	HCT-116	colon:	n/a	chr20:1246967-1246980
35	CTCF	chr20:1246900-1247050	HEK293	kidney:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
36	CTCF	chr20:1246980-1247130	GM06990	blood:	n/a	chr20:1247000-1247013
37	CTCF	chr20:1235537-1235539	GM10248	blood:	n/a	n/a
38	CTCF	chr20:1246920-1247070	AG10803	skin:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
39	CTCF	chr20:1246880-1247030	HUVEC	blood vessel:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
40	CTCF	chr20:1246982-1247032	GM10248	blood:	n/a	chr20:1247000-1247013
41	CTCF	chr20:1243980-1244130	NHLF	lung:	n/a	n/a
42	CTCF	chr20:1246702-1247065	K562	blood:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
43	CTCF	chr20:1247006-1247040	Fibrobl	skin:	n/a	n/a
44	CTCF	chr20:1237126-1237173	ProgFib	skin:	n/a	n/a
45	CTCF	chr20:1246820-1246970	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr20:1246880-1247030	GM12866	blood:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
47	CTCF	chr20:1246900-1247050	AoAF	blood vessel:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
48	CTCF	chr20:1246920-1247070	HCPEpiC	choroid plexus:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
49	CTCF	chr20:1246940-1247090	BJ	skin:	n/a	chr20:1247000-1247013 chr20:1246967-1246980
50	CTCF	chr20:1246900-1247050	HRE	kidney:	n/a	chr20:1247000-1247013 chr20:1246967-1246980

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1246715-1246765	HRPEpiC	eye:	n/a
2	chr20:1246703-1246753	HAEpiC	amniotic membrane:	n/a
3	chr20:1246779-1246829	HIPEpiC	eye:	n/a
4	chr20:1246100-1246150	NHBE	bronchial:	n/a
5	chr20:1246703-1246753	T-47D	breast:	n/a
6	chr20:1246715-1246765	HCT-116	colon:	n/a
7	chr20:1246715-1246765	CMK	blood:	n/a
8	chr20:1246703-1246753	CMK	blood:	n/a
9	chr20:1246703-1246753	HCT-116	colon:	n/a
10	chr20:1246703-1246753	AG09309	skin:	n/a
11	chr20:1246772-1246822	U87	brain:	n/a
12	chr20:1246100-1246150	GM12878	blood:	n/a
13	chr20:1246934-1246984	SKMC	muscle:	n/a
14	chr20:1246715-1246765	ProgFib	skin:	n/a
15	chr20:1246934-1246984	AoSMC	blood vessel:	n/a
16	chr20:1246779-1246829	SK-N-SH	brain:	n/a
17	chr20:1246934-1246984	HPAEpiC	pulmonary alveolar:	n/a
18	chr20:1246779-1246829	NB4	blood:	n/a
19	chr20:1246769-1246819	HIPEpiC	eye:	n/a
20	chr20:1246769-1246819	AG09319	gingival:	n/a
21	chr20:1243523-1243573	HRPEpiC	eye:	n/a
22	chr20:1246769-1246819	ovcar-3	ovarian:	n/a
23	chr20:1243523-1243573	PrEC	prostate:	n/a
24	chr20:1246769-1246819	SK-N-SH	brain:	n/a
25	chr20:1246772-1246822	ovcar-3	ovarian:	n/a
26	chr20:1246100-1246150	SK-N-MC	brain:	n/a
27	chr20:1246769-1246819	HepG2	liver:	n/a
28	chr20:1246100-1246150	PrEC	prostate:	n/a
29	chr20:1246100-1246150	MCF-7	breast:	n/a
30	chr20:1246715-1246765	H1-hESC	embryonic stem cell:	embryo
31	chr20:1246715-1246765	K562	blood:	n/a
32	chr20:1243523-1243573	RPTEC	kidney:	n/a
33	chr20:1246715-1246765	GM12892	blood:	n/a
34	chr20:1246703-1246753	Caco-2	colon:	n/a
35	chr20:1246703-1246753	HPAEpiC	pulmonary alveolar:	n/a
36	chr20:1246715-1246765	HIPEpiC	eye:	n/a
37	chr20:1246934-1246984	BE2_C	brain:	n/a
38	chr20:1246779-1246829	Hepatocyte	liver:	n/a
39	chr20:1246769-1246819	HCM	heart:	n/a
40	chr20:1246769-1246819	HRPEpiC	eye:	n/a
41	chr20:1246715-1246765	Hepatocyte	liver:	n/a
42	chr20:1246772-1246822	SKMC	muscle:	n/a
43	chr20:1246715-1246765	HEEpiC	esophagus:	n/a
44	chr20:1246779-1246829	CMK	blood:	n/a
45	chr20:1246772-1246822	Jurkat	blood:	n/a
46	chr20:1243523-1243573	PFSK-1	brain:	n/a
47	chr20:1246703-1246753	LNCaP	prostate:	n/a
48	chr20:1246100-1246150	PFSK-1	brain:	n/a
49	chr20:1246100-1246150	Hepatocyte	liver:	n/a
50	chr20:1243523-1243573	HRE	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:1204614..1208313-chr20:1245857..1250887,4	K562	blood:
2	chr20:633104..634998-chr20:1246105..1248133,2	K562	blood:
3	chr20:1233558..1237578-chr20:1245297..1248441,5	K562	blood:
4	chr20:1229929..1231590-chr20:1232028..1234534,2	MCF-7	breast:
5	chr20:1206512..1208051-chr20:1245857..1247433,2	K562	blood:
6	chr20:1206971..1208847-chr20:1236164..1237785,2	K562	blood:
7	chr20:1207162..1208733-chr20:1230513..1232075,2	K562	blood:
8	chr20:1229929..1231590-chr20:1232028..1234534,2	MCF-7	breast:
9	chr20:1227236..1231835-chr20:1234457..1238851,4	K562	blood:
10	chr20:1225301..1227153-chr20:1230056..1231608,2	K562	blood:
11	chr20:1206486..1210181-chr20:1234837..1238465,3	K562	blood:
12	chr20:1227236..1231835-chr20:1234457..1238851,4	K562	blood:
13	chr20:1222483..1224322-chr20:1230629..1233078,2	K562	blood:
14	chr20:1205836..1208662-chr20:1230513..1232350,2	K562	blood:
15	chr20:1231093..1233366-chr20:1309666..1311809,2	K562	blood:
16	chr20:1218124..1220880-chr20:1235960..1237512,2	K562	blood:
17	chr20:1234965..1237680-chr20:1245732..1247732,2	K562	blood:
18	chr20:1223258..1226801-chr20:1228440..1231608,4	K562	blood:

No data

Variant related genes	Relation type
SNPH	TF binding region
SNPH	CpG island
ENSG00000101298	chromatin interactions
ENSG00000244588	chromatin interactions
ENSG00000271303	chromatin interactions
ENSG00000125775	chromatin interactions

Extended variants
information (count: 527 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17779586	chr20:1230185-1230186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573863433	chr20:1230227-1230228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147952783	chr20:1230263-1230264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141782510	chr20:1230325-1230326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530083800	chr20:1230367-1230368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540609572	chr20:1230408-1230409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553499791	chr20:1230453-1230454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374817474	chr20:1230526-1230527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73604138	chr20:1230528-1230529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs532414676	chr20:1230536-1230537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552473609	chr20:1230542-1230543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569088596	chr20:1230577-1230578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531494429	chr20:1230640-1230641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573326285	chr20:1230647-1230648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545180298	chr20:1230648-1230649	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191197392	chr20:1230649-1230650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568147061	chr20:1230656-1230657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111883306	chr20:1230673-1230674	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116863079	chr20:1230688-1230689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs372305530	chr20:1230732-1230733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376657297	chr20:1230740-1230741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73604141	chr20:1230745-1230746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558782952	chr20:1230806-1230807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149167030	chr20:1230849-1230850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184618528	chr20:1230855-1230856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561274945	chr20:1230876-1230877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs143264923	chr20:1230890-1230891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs203528	chr20:1230904-1230905	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs73604145	chr20:1231005-1231006	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs73604146	chr20:1231013-1231014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs73604147	chr20:1231024-1231025	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115863801	chr20:1231034-1231035	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560558165	chr20:1231045-1231046	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs73604148	chr20:1231082-1231083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369836691	chr20:1231200-1231201	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs141396125	chr20:1231242-1231243	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559285018	chr20:1231312-1231313	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529689217	chr20:1231354-1231355	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548863665	chr20:1231359-1231360	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs16992790	chr20:1231418-1231419	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562728501	chr20:1231428-1231429	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs190349558	chr20:1231462-1231463	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs528144849	chr20:1231469-1231470	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs193302532	chr20:1231487-1231488	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs116887559	chr20:1231519-1231520	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546927952	chr20:1231523-1231524	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527402388	chr20:1231615-1231616	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs203529	chr20:1231683-1231684	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570433948	chr20:1231746-1231747	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs144915820	chr20:1231771-1231772	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1229200-1233200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr20:1229600-1232800	Weak transcription	K562	blood
3	chr20:1231400-1232000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
4	chr20:1231400-1232200	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr20:1231600-1232200	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr20:1231600-1232200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr20:1231600-1232400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr20:1231800-1232000	Enhancers	HUVEC	blood vessel
9	chr20:1232800-1233200	Enhancers	K562	blood
10	chr20:1233200-1233600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr20:1233200-1233600	Flanking Active TSS	K562	blood
12	chr20:1233600-1235000	Enhancers	K562	blood
13	chr20:1234400-1235600	Enhancers	Fetal Lung	lung
14	chr20:1235000-1235400	Flanking Active TSS	K562	blood
15	chr20:1235200-1235400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr20:1235400-1236600	Enhancers	K562	blood
17	chr20:1236000-1236600	Enhancers	HUVEC	blood vessel
18	chr20:1236600-1237200	ZNF genes & repeats	K562	blood
19	chr20:1238000-1239000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr20:1239000-1239800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr20:1242400-1244200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr20:1243000-1245600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr20:1243400-1245400	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr20:1243400-1246200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr20:1243400-1246400	Enhancers	Primary T cells fromperipheralblood	blood
26	chr20:1243600-1245800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr20:1243800-1244000	Enhancers	K562	blood
28	chr20:1243800-1246000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr20:1243800-1246000	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr20:1244000-1244200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr20:1244000-1244200	Flanking Active TSS	K562	blood
32	chr20:1244000-1244400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr20:1244000-1244600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr20:1244000-1245800	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr20:1244200-1244400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr20:1244200-1244400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr20:1244200-1244400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr20:1244200-1244600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr20:1244200-1244800	Enhancers	K562	blood
40	chr20:1244200-1246200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr20:1244400-1244600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr20:1244400-1244600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr20:1244400-1245600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr20:1244400-1245800	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr20:1244400-1246000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr20:1244400-1246200	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr20:1244400-1246200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr20:1244600-1244800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr20:1244600-1245600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr20:1244600-1246000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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