Variant report

Variant	esv2754411
Chromosome Location	chr1:215235605-215281605
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:430)
CpG islands
(count:917)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:215274898-215275032	K562	blood:	n/a	n/a
2	ATF1	chr1:215252670-215252769	K562	blood:	n/a	n/a
3	CEBPB	chr1:215274822-215275151	IMR90	lung:	n/a	chr1:215274975-215274986
4	CEBPB	chr1:215244919-215245194	IMR90	lung:	n/a	chr1:215245042-215245053
5	CEBPB	chr1:215274907-215275125	K562	blood:	n/a	chr1:215274975-215274986
6	CEBPB	chr1:215274812-215275154	A549	lung:	n/a	chr1:215274975-215274986
7	CEBPB	chr1:215243144-215243320	A549	lung:	n/a	n/a
8	CEBPB	chr1:215250259-215250459	HepG2	liver:	n/a	chr1:215250341-215250352
9	CEBPB	chr1:215244913-215245192	HepG2	liver:	n/a	chr1:215245042-215245053
10	CEBPB	chr1:215256809-215257090	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:215274818-215275170	HepG2	liver:	n/a	chr1:215274975-215274986
12	CHD2	chr1:215255939-215256139	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr1:215266467-215266519	K562	blood:	n/a	n/a
14	CTBP2	chr1:215255151-215256317	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr1:215249800-215249950	AG04449	skin:	n/a	n/a
16	CTCF	chr1:215249800-215249950	SAEC	small airway:	n/a	n/a
17	CTCF	chr1:215249820-215249970	HPF	lung:	n/a	n/a
18	CTCF	chr1:215256016-215256037	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr1:215249780-215249930	Caco-2	colon:	n/a	n/a
20	CTCF	chr1:215249720-215249870	GM12874	blood:	n/a	n/a
21	CTCF	chr1:215256001-215256144	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:215255920-215256070	AG04449	skin:	n/a	n/a
23	CTCF	chr1:215249780-215249930	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr1:215249760-215249910	HCM	heart:	n/a	n/a
25	CTCF	chr1:215255660-215255810	AG04449	skin:	n/a	n/a
26	CTCF	chr1:215249820-215249970	GM12866	blood:	n/a	n/a
27	CTCF	chr1:215249498-215250063	SK-N-SH	brain:	n/a	n/a
28	CTCF	chr1:215249741-215249978	ECC-1	luminal epithelium:	n/a	n/a
29	CTCF	chr1:215255980-215256130	HAc	cerebellar:	n/a	n/a
30	CTCF	chr1:215249780-215249930	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr1:215255980-215256130	HMF	breast:	n/a	n/a
32	CTCF	chr1:215249760-215249910	GM12864	blood:	n/a	n/a
33	CTCF	chr1:215249780-215249930	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr1:215249760-215249910	AG10803	skin:	n/a	n/a
35	CTCF	chr1:215249725-215249986	Gliobla	brain:	n/a	n/a
36	CTCF	chr1:215255960-215256110	AG04449	skin:	n/a	n/a
37	CTCF	chr1:215249800-215249950	Caco-2	colon:	n/a	n/a
38	CTCF	chr1:215249770-215249952	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr1:215249671-215250031	K562	blood:	n/a	n/a
40	CTCF	chr1:215249718-215249980	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:215249800-215249950	BE2_C	brain:	n/a	n/a
42	CTCF	chr1:215249780-215249930	GM06990	blood:	n/a	n/a
43	CTCF	chr1:215249760-215249910	GM12873	blood:	n/a	n/a
44	CTCF	chr1:215255880-215256030	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr1:215249780-215249930	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr1:215249720-215249870	GM12866	blood:	n/a	n/a
47	CTCF	chr1:215249780-215249930	HMEC	breast:	n/a	n/a
48	CTCF	chr1:215249780-215249930	BJ	skin:	n/a	n/a
49	CTCF	chr1:215249800-215249950	GM12868	blood:	n/a	n/a
50	CTCF	chr1:215249800-215249950	HL-60	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:215256745-215256795	HCT-116	colon:	n/a
2	chr1:215256448-215256498	MCF-7	breast:	n/a
3	chr1:215256745-215256795	HCT-116	colon:	n/a
4	chr1:215256448-215256498	MCF-7	breast:	n/a
5	chr1:215257222-215257272	SK-N-SH	brain:	n/a
6	chr1:215256262-215256312	MCF-7	breast:	n/a
7	chr1:215256745-215256795	Jurkat	blood:	n/a
8	chr1:215256451-215256501	NHDF-neo	bronchial:	n/a
9	chr1:215256262-215256312	H1-hESC	embryonic stem cell:	embryo
10	chr1:215255110-215255160	ECC-1	luminal epithelium:	n/a
11	chr1:215255572-215255622	Caco-2	colon:	n/a
12	chr1:215256451-215256501	SK-N-MC	brain:	n/a
13	chr1:215255110-215255160	HMEC	breast:	n/a
14	chr1:215256635-215256685	SKMC	muscle:	n/a
15	chr1:215256448-215256498	AG10803	skin:	n/a
16	chr1:215256887-215256937	GM12891	blood:	n/a
17	chr1:215259771-215259821	NB4	blood:	n/a
18	chr1:215256745-215256795	T-47D	breast:	n/a
19	chr1:215256978-215257028	PFSK-1	brain:	n/a
20	chr1:215256978-215257028	NHDF-neo	bronchial:	n/a
21	chr1:215255716-215255766	AoSMC	blood vessel:	n/a
22	chr1:215255572-215255622	GM12892	blood:	n/a
23	chr1:215259771-215259821	BJ	skin:	n/a
24	chr1:215256635-215256685	MCF-7	breast:	n/a
25	chr1:215256887-215256937	PFSK-1	brain:	n/a
26	chr1:215256887-215256937	HEK293	kidney:	embryo
27	chr1:215256451-215256501	LNCaP	prostate:	n/a
28	chr1:215255716-215255766	HepG2	liver:	n/a
29	chr1:215255572-215255622	AoSMC	blood vessel:	n/a
30	chr1:215256870-215256920	HMEC	breast:	n/a
31	chr1:215256745-215256795	NT2-D1	testis:	n/a
32	chr1:215256745-215256795	GM12892	blood:	n/a
33	chr1:215256448-215256498	Caco-2	colon:	n/a
34	chr1:215259771-215259821	HCPEpiC	choroid plexus:	n/a
35	chr1:215255572-215255622	RPTEC	kidney:	n/a
36	chr1:215259771-215259821	HCT-116	colon:	n/a
37	chr1:215256870-215256920	MCF-7	breast:	n/a
38	chr1:215256448-215256498	PFSK-1	brain:	n/a
39	chr1:215256451-215256501	Caco-2	colon:	n/a
40	chr1:215256451-215256501	NHBE	bronchial:	n/a
41	chr1:215256870-215256920	HRPEpiC	eye:	n/a
42	chr1:215255161-215255211	Hepatocyte	liver:	n/a
43	chr1:215255716-215255766	HMEC	breast:	n/a
44	chr1:215256887-215256937	NT2-D1	testis:	n/a
45	chr1:215256451-215256501	A549	lung:	n/a
46	chr1:215255572-215255622	U87	brain:	n/a
47	chr1:215256451-215256501	SKMC	muscle:	n/a
48	chr1:215256254-215256304	A549	lung:	n/a
49	chr1:215259771-215259821	ProgFib	skin:	n/a
50	chr1:215256635-215256685	IMR90	lung:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:215280557..215283652-chr1:215283955..215286310,3	MCF-7	breast:
2	chr1:214833954..214834916-chr1:215249431..215250403,7	MCF-7	breast:
3	chr1:215249267..215251952-chr1:215286200..215288230,2	MCF-7	breast:
4	chr1:215196838..215197537-chr1:215249583..215250160,2	MCF-7	breast:
5	chr1:215249732..215252476-chr1:215255654..215258556,2	K562	blood:
6	chr1:215259190..215261920-chr1:215262011..215264888,2	MCF-7	breast:
7	chr1:215259190..215261920-chr1:215262011..215264888,2	MCF-7	breast:
8	chr1:214831928..214832819-chr1:215249703..215250277,2	MCF-7	breast:
9	chr1:214773067..214775005-chr1:215239783..215241407,2	K562	blood:
10	chr1:215125951..215126692-chr1:215249388..215250381,2	MCF-7	breast:
11	chr1:214981872..214982949-chr1:215249210..215250250,4	MCF-7	breast:
12	chr1:215163670..215166597-chr1:215252249..215254651,2	MCF-7	breast:
13	chr1:215249022..215252957-chr1:215253448..215258066,5	MCF-7	breast:

No data

Variant related genes	Relation type
KCNK2	TF binding region
KCNK2	CpG island
ENSG00000082482	chromatin interactions

Extended variants
information (count: 1678 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1678 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10864148	chr1:215235649-215235650	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144657373	chr1:215235653-215235654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569321393	chr1:215235669-215235670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185646596	chr1:215235671-215235672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548711272	chr1:215235681-215235682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs61818279	chr1:215235697-215235698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534427922	chr1:215235729-215235730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554101581	chr1:215235738-215235739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577355720	chr1:215235782-215235783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371759946	chr1:215235795-215235796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34377326	chr1:215235877-215235878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556433855	chr1:215235883-215235884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574894647	chr1:215235899-215235900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138618853	chr1:215235927-215235928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557517855	chr1:215235941-215235942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574926102	chr1:215235985-215235986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374699993	chr1:215236008-215236009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368852010	chr1:215236009-215236010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371097316	chr1:215236019-215236020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577408415	chr1:215236055-215236056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540299760	chr1:215236065-215236066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560122909	chr1:215236080-215236081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74140901	chr1:215236119-215236120	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs149243599	chr1:215236132-215236133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12038094	chr1:215236196-215236197	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs531755254	chr1:215236197-215236198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548576832	chr1:215236202-215236203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568444206	chr1:215236285-215236286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190408405	chr1:215236322-215236323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371690791	chr1:215236406-215236407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573382713	chr1:215236418-215236419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114304868	chr1:215236432-215236433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556446458	chr1:215236445-215236446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374977586	chr1:215236462-215236463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537468773	chr1:215236486-215236487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367760305	chr1:215236487-215236488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76891756	chr1:215236488-215236489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542207756	chr1:215236528-215236529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539994063	chr1:215236535-215236536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553784405	chr1:215236552-215236553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182285648	chr1:215236563-215236564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545987329	chr1:215236565-215236566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562794703	chr1:215236577-215236578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574651790	chr1:215236582-215236583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375915959	chr1:215236619-215236620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531667353	chr1:215236649-215236650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113024785	chr1:215236664-215236665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75066696	chr1:215236710-215236711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144417713	chr1:215236711-215236712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111795875	chr1:215236752-215236753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215222800-215242200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:215228000-215237200	Weak transcription	Pancreas	Pancrea
3	chr1:215229200-215237800	Weak transcription	NHEK	skin
4	chr1:215229400-215253000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:215231600-215247600	Weak transcription	NHDF-Ad	bronchial
6	chr1:215234000-215237800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:215235800-215236400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:215236600-215237200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr1:215237600-215238200	Enhancers	HMEC	breast
10	chr1:215237800-215238200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr1:215237800-215238200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:215237800-215238200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:215237800-215238400	Enhancers	NHEK	skin
14	chr1:215242200-215242400	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr1:215247600-215248200	Strong transcription	NHDF-Ad	bronchial
16	chr1:215248200-215252600	Weak transcription	NHDF-Ad	bronchial
17	chr1:215250200-215250600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr1:215252600-215254200	Enhancers	NHDF-Ad	bronchial
19	chr1:215253000-215253400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:215253200-215253400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:215253400-215254400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:215253400-215255000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:215254000-215254200	Enhancers	Fetal Brain Female	brain
24	chr1:215254000-215255000	Enhancers	Osteobl	bone
25	chr1:215254200-215254800	Flanking Active TSS	NHDF-Ad	bronchial
26	chr1:215254400-215254600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:215254400-215255000	Enhancers	Fetal Brain Male	brain
28	chr1:215254600-215254800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
29	chr1:215254600-215254800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:215254800-215255000	Active TSS	NHDF-Ad	bronchial
31	chr1:215254800-215255200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
32	chr1:215254800-215255400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:215254800-215255400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:215254800-215257400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
35	chr1:215254800-215257400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr1:215254800-215259000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:215254800-215260000	Active TSS	Fetal Brain Female	brain
38	chr1:215255000-215255200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
39	chr1:215255000-215255200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
40	chr1:215255000-215255200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:215255000-215255200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr1:215255000-215255200	Flanking Active TSS	Fetal Brain Male	brain
43	chr1:215255000-215255200	Active TSS	NH-A	brain
44	chr1:215255000-215255200	Flanking Active TSS	NHDF-Ad	bronchial
45	chr1:215255000-215255200	Active TSS	NHLF	lung
46	chr1:215255000-215255400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:215255000-215255400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:215255000-215255400	Active TSS	Brain Germinal Matrix	brain
49	chr1:215255000-215255400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
50	chr1:215255000-215255400	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain

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