Variant report

Variant	nsv877728
Chromosome Location	chr3:162085820-162236885
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:491)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:162155356-162155600	K562	blood:	n/a	n/a
2	ATF1	chr3:162196526-162196643	K562	blood:	n/a	n/a
3	ATF3	chr3:162210124-162210804	A549	lung:	n/a	n/a
4	BACH1	chr3:162086751-162086794	K562	blood:	n/a	n/a
5	BACH1	chr3:162205043-162205091	H1-hESC	embryonic stem cell:	n/a	chr3:162205077-162205091
6	BCL3	chr3:162210121-162210895	A549	lung:	n/a	n/a
7	BHLHE40	chr3:162096654-162096707	GM12878	blood:	n/a	n/a
8	CBX3	chr3:162108559-162109098	HCT-116	colon:	n/a	n/a
9	CCNT2	chr3:162113799-162113999	K562	blood:	n/a	n/a
10	CEBPB	chr3:162210151-162210916	A549	lung:	n/a	chr3:162210491-162210504
11	CEBPB	chr3:162108642-162109478	IMR90	lung:	n/a	n/a
12	CEBPB	chr3:162209758-162210932	A549	lung:	n/a	chr3:162210491-162210504
13	CEBPB	chr3:162209757-162210919	IMR90	lung:	n/a	chr3:162210491-162210504
14	CEBPB	chr3:162151375-162151576	HepG2	liver:	n/a	chr3:162151476-162151487
15	CEBPB	chr3:162219255-162219607	HepG2	liver:	n/a	chr3:162219429-162219440
16	CEBPB	chr3:162219243-162219812	A549	lung:	n/a	chr3:162219429-162219440
17	CEBPB	chr3:162209719-162210974	Hela-S3	cervix:	n/a	chr3:162210491-162210504
18	CEBPB	chr3:162112546-162112549	A549	lung:	n/a	n/a
19	CEBPB	chr3:162209739-162210089	MCF-7	breast:	n/a	n/a
20	CEBPB	chr3:162088054-162088329	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:162088084-162088369	IMR90	lung:	n/a	n/a
22	CEBPB	chr3:162219267-162219549	K562	blood:	n/a	chr3:162219429-162219440
23	CEBPB	chr3:162209752-162210155	MCF-7	breast:	n/a	n/a
24	CEBPB	chr3:162219248-162219620	IMR90	lung:	n/a	chr3:162219429-162219440
25	CEBPB	chr3:162177204-162177284	H1-hESC	embryonic stem cell:	n/a	chr3:162177255-162177266
26	CEBPB	chr3:162108710-162109493	A549	lung:	n/a	n/a
27	CEBPB	chr3:162205022-162205310	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:162209674-162210107	A549	lung:	n/a	n/a
29	CEBPB	chr3:162177135-162177440	HepG2	liver:	n/a	chr3:162177255-162177266
30	CEBPB	chr3:162209604-162211122	A549	lung:	n/a	chr3:162210491-162210504
31	CTCF	chr3:162207705-162207892	T-47D	breast:	n/a	n/a
32	CTCF	chr3:162136120-162136270	HCT-116	colon:	n/a	n/a
33	CTCF	chr3:162118644-162118734	Gliobla	brain:	n/a	n/a
34	CTCF	chr3:162207725-162207920	GM12878	blood:	n/a	n/a
35	CTCF	chr3:162207800-162207950	AG10803	skin:	n/a	n/a
36	CTCF	chr3:162207860-162208010	RPTEC	kidney:	n/a	n/a
37	CTCF	chr3:162207742-162207875	Fibrobl	skin:	n/a	n/a
38	CTCF	chr3:162207840-162207990	HFF	foreskin:	n/a	n/a
39	CTCF	chr3:162136054-162136221	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:162118644-162118821	GM12878	blood:	n/a	n/a
41	CTCF	chr3:162221103-162221152	LNCaP	prostate:	n/a	n/a
42	CTCF	chr3:162207640-162207790	BE2_C	brain:	n/a	n/a
43	CTCF	chr3:162136040-162136190	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr3:162207800-162207950	HVMF	connective:	n/a	n/a
45	CTCF	chr3:162207728-162207935	LNCaP	prostate:	n/a	n/a
46	CTCF	chr3:162207760-162207910	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr3:162136124-162136200	LNCaP	prostate:	n/a	n/a
48	CTCF	chr3:162215024-162215029	GM13976	blood:	n/a	n/a
49	CTCF	chr3:162208829-162208892	A549	lung:	n/a	n/a
50	CTCF	chr3:162234916-162235212	IMR90	lung:	n/a	chr3:162235077-162235098 chr3:162235075-162235093

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:162210236-162210286	SK-N-SH	brain:	n/a
2	chr3:162210236-162210286	SK-N-SH	brain:	n/a
3	chr3:162210236-162210286	K562	blood:	n/a
4	chr3:162129530-162129580	IMR90	lung:	fetal
5	chr3:162129530-162129580	SAEC	small airway:	n/a
6	chr3:162129530-162129580	HMEC	breast:	n/a
7	chr3:162210236-162210286	AG10803	skin:	n/a
8	chr3:162210236-162210286	HRE	kidney:	n/a
9	chr3:162129530-162129580	AG09309	skin:	n/a
10	chr3:162129530-162129580	ECC-1	luminal epithelium:	n/a
11	chr3:162210236-162210286	GM06990	blood:	n/a
12	chr3:162129530-162129580	T-47D	breast:	n/a
13	chr3:162129530-162129580	NB4	blood:	n/a
14	chr3:162210236-162210286	MCF-7	breast:	n/a
15	chr3:162210236-162210286	GM19239	blood:	n/a
16	chr3:162129530-162129580	ProgFib	skin:	n/a
17	chr3:162210236-162210286	HCF	heart:	n/a
18	chr3:162129530-162129580	GM12891	blood:	n/a
19	chr3:162129530-162129580	MCF10A-Er-Src	breast:	n/a
20	chr3:162129530-162129580	PrEC	prostate:	n/a
21	chr3:162210236-162210286	HRPEpiC	eye:	n/a
22	chr3:162129530-162129580	HUVEC	blood vessel:	n/a
23	chr3:162129530-162129580	PFSK-1	brain:	n/a
24	chr3:162210236-162210286	ovcar-3	ovarian:	n/a
25	chr3:162210236-162210286	RPTEC	kidney:	n/a
26	chr3:162129530-162129580	GM12878	blood:	n/a
27	chr3:162129530-162129580	Jurkat	blood:	n/a
28	chr3:162210236-162210286	HUVEC	blood vessel:	n/a
29	chr3:162210236-162210286	GM12891	blood:	n/a
30	chr3:162129530-162129580	H1-hESC	embryonic stem cell:	embryo
31	chr3:162129530-162129580	HRCEpiC	kidney:	n/a
32	chr3:162129530-162129580	HCPEpiC	choroid plexus:	n/a
33	chr3:162210236-162210286	HMEC	breast:	n/a
34	chr3:162210236-162210286	H1-hESC	embryonic stem cell:	embryo
35	chr3:162210236-162210286	GM12878	blood:	n/a
36	chr3:162210236-162210286	HCT-116	colon:	n/a
37	chr3:162129530-162129580	SKMC	muscle:	n/a
38	chr3:162129530-162129580	SK-N-MC	brain:	n/a
39	chr3:162210236-162210286	T-47D	breast:	n/a
40	chr3:162129530-162129580	HIPEpiC	eye:	n/a
41	chr3:162129530-162129580	HL-60	blood:	n/a
42	chr3:162129530-162129580	HCF	heart:	n/a
43	chr3:162129530-162129580	AG09319	gingival:	n/a
44	chr3:162129530-162129580	HepG2	liver:	n/a
45	chr3:162210236-162210286	HCPEpiC	choroid plexus:	n/a
46	chr3:162210236-162210286	SK-N-MC	brain:	n/a
47	chr3:162129530-162129580	HRE	kidney:	n/a
48	chr3:162210236-162210286	HL-60	blood:	n/a
49	chr3:162210236-162210286	AoSMC	blood vessel:	n/a
50	chr3:162129530-162129580	SK-N-SH	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:162236582..162237488-chr4:38505086..38506008,2	MCF-7	breast:
2	chr3:162161201..162163178-chr3:162177234..162178956,2	MCF-7	breast:
3	chr3:162084506..162087458-chr3:162087812..162089576,2	MCF-7	breast:
4	chr3:162084506..162087458-chr3:162087812..162089576,2	MCF-7	breast:
5	chr3:162215860..162218810-chr3:162234701..162237384,2	K562	blood:
6	chr3:162215860..162218810-chr3:162234701..162237384,2	K562	blood:
7	chr3:162118223..162119105-chr3:162517137..162517997,2	MCF-7	breast:
8	chr3:162122033..162123865-chr3:162146680..162148744,2	K562	blood:
9	chr3:162122033..162123865-chr3:162146680..162148744,2	K562	blood:
10	chr3:162161201..162163178-chr3:162177234..162178956,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTSSB-7	chr3:162204329-162204737	NONHSAT093022

No data

Variant related genes	Relation type
TOMM22P6	TF binding region
TOMM22P6	CpG island

Extended variants
information (count: 1882 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1882 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12488754	chr3:162085820-162085821	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528161562	chr3:162085827-162085828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs36007688	chr3:162085879-162085880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182854423	chr3:162085880-162085881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12486036	chr3:162085905-162085906	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs12486096	chr3:162086033-162086034	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs550902125	chr3:162086063-162086064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9813509	chr3:162086083-162086084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571077626	chr3:162086104-162086105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539766962	chr3:162086105-162086106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546555607	chr3:162086114-162086115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375024807	chr3:162086158-162086159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543165019	chr3:162086174-162086175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76637976	chr3:162086176-162086177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535604411	chr3:162086185-162086186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573196321	chr3:162086201-162086202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576526386	chr3:162086207-162086208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575690653	chr3:162086236-162086237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149795193	chr3:162086247-162086248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556882225	chr3:162086251-162086252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187585915	chr3:162086255-162086256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192395753	chr3:162086266-162086267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146822567	chr3:162086305-162086306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139652626	chr3:162086338-162086339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs16848359	chr3:162086339-162086340	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs144407433	chr3:162086367-162086368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530523717	chr3:162086418-162086419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184176664	chr3:162086448-162086449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564540486	chr3:162086449-162086450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs16848362	chr3:162086467-162086468	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs532395265	chr3:162086469-162086470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545374185	chr3:162086494-162086495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566869779	chr3:162086500-162086501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374162302	chr3:162086513-162086514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535449726	chr3:162086524-162086525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149805303	chr3:162086571-162086572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562964836	chr3:162086585-162086586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74722805	chr3:162086599-162086600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200029011	chr3:162086645-162086646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201053258	chr3:162086653-162086654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530142080	chr3:162086654-162086655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201339983	chr3:162086655-162086656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201613463	chr3:162086656-162086657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568786923	chr3:162086657-162086658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140401041	chr3:162086658-162086659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569290117	chr3:162086694-162086695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559103351	chr3:162086711-162086712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557088341	chr3:162086714-162086715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570647854	chr3:162086735-162086736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543768188	chr3:162086737-162086738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162082800-162088400	Enhancers	Fetal Heart	heart
2	chr3:162083200-162086400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:162083200-162087800	Enhancers	Fetal Stomach	stomach
4	chr3:162083600-162086600	Enhancers	Fetal Lung	lung
5	chr3:162083800-162086400	Enhancers	Fetal Kidney	kidney
6	chr3:162084000-162087400	Enhancers	Rectal Smooth Muscle	rectum
7	chr3:162084200-162086000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr3:162084400-162087000	Enhancers	Colon Smooth Muscle	Colon
9	chr3:162085000-162087200	Weak transcription	Dnd41	blood
10	chr3:162085200-162086400	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr3:162085400-162086000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:162085400-162086000	Weak transcription	Fetal Brain Male	brain
13	chr3:162085400-162086400	Enhancers	Placenta Amnion	Placenta Amnion
14	chr3:162085400-162086400	Enhancers	Psoas Muscle	Psoas
15	chr3:162085600-162086000	Enhancers	Brain Cingulate Gyrus	brain
16	chr3:162085600-162086000	Enhancers	Stomach Smooth Muscle	stomach
17	chr3:162085600-162086000	Enhancers	NHLF	lung
18	chr3:162085600-162086200	Enhancers	Brain Hippocampus Middle	brain
19	chr3:162085600-162086400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr3:162085600-162086400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr3:162085600-162086400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr3:162085600-162086400	Enhancers	Brain Germinal Matrix	brain
23	chr3:162085600-162087400	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr3:162085800-162086400	Enhancers	Fetal Muscle Leg	muscle
25	chr3:162085800-162086400	Enhancers	Small Intestine	intestine
26	chr3:162086000-162086200	Enhancers	HSMMtube	muscle
27	chr3:162086000-162086400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:162086000-162086400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr3:162086000-162086600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:162086000-162087000	Weak transcription	Stomach Smooth Muscle	stomach
31	chr3:162086000-162087200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr3:162086000-162088400	Enhancers	Fetal Brain Male	brain
33	chr3:162086200-162086400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr3:162086400-162087000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr3:162086400-162087600	Weak transcription	HSMMtube	muscle
36	chr3:162086400-162087800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr3:162086400-162088000	Weak transcription	Psoas Muscle	Psoas
38	chr3:162087000-162089000	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr3:162087200-162087400	Enhancers	Stomach Smooth Muscle	stomach
40	chr3:162087200-162089800	Enhancers	Dnd41	blood
41	chr3:162087600-162088600	Enhancers	HSMM	muscle
42	chr3:162087600-162089000	Enhancers	HSMMtube	muscle
43	chr3:162087800-162088200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr3:162087800-162088600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:162087800-162088800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr3:162087800-162089000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:162088000-162088200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr3:162088000-162088200	Enhancers	Psoas Muscle	Psoas
49	chr3:162088000-162088400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr3:162088000-162089000	Enhancers	H9 Cell Line	embryonic stem cell

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