Variant report

Variant	nsv875346
Chromosome Location	chr2:160965335-161044155
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:651)
CpG islands
(count:0)
Chromatin interactive
region (count:80)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:160966482-160966795	HepG2	liver:	n/a	n/a
2	ATF2	chr2:160968650-160969144	GM12878	blood:	n/a	n/a
3	BATF	chr2:160968776-160969110	GM12878	blood:	n/a	n/a
4	BATF	chr2:160968686-160969071	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:160968700-160969078	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:160968807-160969070	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:160968635-160969253	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:160966521-160966814	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:161004753-161004929	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:160990249-160990273	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:160990172-160990291	A549	lung:	n/a	n/a
12	CEBPB	chr2:161014455-161014697	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:160965963-160966725	A549	lung:	n/a	chr2:160966306-160966317
14	CEBPB	chr2:161028116-161028396	A549	lung:	n/a	chr2:161028232-161028243
15	CEBPB	chr2:160966138-160966335	K562	blood:	n/a	chr2:160966306-160966317
16	CEBPB	chr2:160998351-160998833	MCF-7	breast:	n/a	n/a
17	CEBPB	chr2:160998474-160998688	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:161022533-161022960	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:160965965-160966662	HepG2	liver:	n/a	chr2:160966306-160966317
20	CEBPB	chr2:160998326-160998838	MCF-7	breast:	n/a	n/a
21	CEBPB	chr2:161036870-161037029	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:160993909-160994075	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:161005121-161005299	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:161028117-161028337	IMR90	lung:	n/a	chr2:161028232-161028243
25	CEBPB	chr2:160966016-160966681	IMR90	lung:	n/a	chr2:160966306-160966317
26	CEBPB	chr2:161028096-161028400	HepG2	liver:	n/a	chr2:161028232-161028243
27	CEBPB	chr2:160966266-160966735	H1-hESC	embryonic stem cell:	n/a	chr2:160966306-160966317
28	CEBPB	chr2:161022532-161023040	MCF-7	breast:	n/a	n/a
29	CEBPB	chr2:161013175-161013573	IMR90	lung:	n/a	n/a
30	CHD2	chr2:160968788-160969047	GM12878	blood:	n/a	n/a
31	CHD2	chr2:161037792-161037844	HepG2	liver:	n/a	n/a
32	CHD2	chr2:161012732-161012768	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:160966580-160966730	HEK293	kidney:	n/a	n/a
34	CTCF	chr2:160966580-160966730	AG09319	gingival:	n/a	n/a
35	CTCF	chr2:161012620-161012770	WI-38	lung:	n/a	n/a
36	CTCF	chr2:160966540-160966690	AG09309	skin:	n/a	n/a
37	CTCF	chr2:160966580-160966730	NHEK	skin:	n/a	n/a
38	CTCF	chr2:160966580-160966730	BJ	skin:	n/a	n/a
39	CTCF	chr2:161041532-161041616	GM10248	blood:	n/a	n/a
40	CTCF	chr2:160966620-160966770	A549	lung:	n/a	n/a
41	CTCF	chr2:160966540-160966690	HPF	lung:	n/a	n/a
42	CTCF	chr2:160966523-160966785	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:160966440-160966590	HAc	cerebellar:	n/a	n/a
44	CTCF	chr2:160966560-160966710	K562	blood:	n/a	n/a
45	CTCF	chr2:160966580-160966730	GM12875	blood:	n/a	n/a
46	CTCF	chr2:160966249-160966252	GM10266	blood:	n/a	n/a
47	CTCF	chr2:160966540-160966690	AG04450	lung:	n/a	n/a
48	CTCF	chr2:160966526-160966753	GM10248	blood:	n/a	n/a
49	CTCF	chr2:161012680-161012830	Caco-2	colon:	n/a	n/a
50	CTCF	chr2:160966544-160966776	Fibrobl	skin:	n/a	n/a

No data

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:161023086..161025481-chr2:161028463..161031210,2	MCF-7	breast:
2	chr2:160998766..161001076-chr2:161004659..161006213,2	K562	blood:
3	chr2:161022710..161025666-chr2:161026068..161028687,2	MCF-7	breast:
4	chr2:160978525..160981101-chr2:160983731..160985356,2	MCF-7	breast:
5	chr2:160993718..160995794-chr2:160997568..160999439,2	MCF-7	breast:
6	chr2:160982529..160984640-chr2:161078156..161079933,2	MCF-7	breast:
7	chr2:161021190..161023892-chr2:161082656..161085932,3	MCF-7	breast:
8	chr2:161033297..161035700-chr2:161053449..161055429,2	MCF-7	breast:
9	chr2:161012600..161015178-chr2:161083788..161087804,4	MCF-7	breast:
10	chr2:161029423..161031683-chr2:161033296..161035758,2	MCF-7	breast:
11	chr2:160993718..160995794-chr2:160997568..160999439,2	MCF-7	breast:
12	chr2:161000112..161002842-chr2:161027169..161029887,2	MCF-7	breast:
13	chr2:160968652..160971180-chr2:161059515..161062161,2	MCF-7	breast:
14	chr2:161000112..161002842-chr2:161027169..161029887,2	MCF-7	breast:
15	chr2:160981983..160984926-chr2:160986223..160988366,2	K562	blood:
16	chr2:160998766..161001076-chr2:161004659..161006213,2	K562	blood:
17	chr2:161012044..161015956-chr2:161077276..161081023,8	MCF-7	breast:
18	chr2:161027893..161029945-chr2:161054838..161057768,2	MCF-7	breast:
19	chr2:160750717..160753451-chr2:160965407..160967520,2	MCF-7	breast:
20	chr2:160977849..160980752-chr2:161063430..161065626,2	MCF-7	breast:
21	chr2:161011918..161014903-chr2:161016994..161018899,2	K562	blood:
22	chr2:160969923..160971430-chr2:161063576..161065947,2	MCF-7	breast:
23	chr2:161000991..161002542-chr2:161026874..161029211,2	MCF-7	breast:
24	chr2:161019041..161021255-chr2:161080992..161082539,2	MCF-7	breast:
25	chr2:160966151..160967115-chr2:161066856..161067816,4	K562	blood:
26	chr2:161015690..161017268-chr2:161021219..161023930,2	MCF-7	breast:
27	chr2:161014516..161016610-chr2:161055960..161058326,2	MCF-7	breast:
28	chr2:161009313..161012082-chr2:161014084..161016057,3	MCF-7	breast:
29	chr2:161011213..161014505-chr2:161097199..161099716,3	MCF-7	breast:
30	chr2:161017359..161019916-chr2:161083312..161086172,2	MCF-7	breast:
31	chr2:160963372..160965662-chr2:161085963..161088165,2	MCF-7	breast:
32	chr2:161030837..161032857-chr7:104653058..104655508,2	MCF-7	breast:
33	chr2:161022633..161024812-chr2:161077424..161079936,2	MCF-7	breast:
34	chr2:160981270..160984730-chr2:160985198..160987380,3	MCF-7	breast:
35	chr2:161011444..161016530-chr2:161074862..161081219,9	MCF-7	breast:
36	chr2:161029621..161032240-chr2:161097556..161099652,2	MCF-7	breast:
37	chr2:160978525..160981101-chr2:160983731..160985356,2	MCF-7	breast:
38	chr2:161022710..161025666-chr2:161026068..161028687,2	MCF-7	breast:
39	chr2:161025898..161028586-chr2:161060919..161062605,2	MCF-7	breast:
40	chr2:161011705..161015715-chr2:161083220..161088389,8	MCF-7	breast:
41	chr2:160994975..160996748-chr2:161076559..161078782,2	MCF-7	breast:
42	chr2:161021794..161024163-chr2:161085942..161087793,2	MCF-7	breast:
43	chr2:160997193..161000864-chr2:161081939..161085480,4	MCF-7	breast:
44	chr2:161011891..161014884-chr2:161060421..161064713,4	MCF-7	breast:
45	chr2:160966552..160967071-chr2:161066902..161067530,2	MCF-7	breast:
46	chr2:161029423..161031683-chr2:161033296..161035758,2	MCF-7	breast:
47	chr2:161023206..161025087-chr2:161054934..161056885,2	MCF-7	breast:
48	chr2:160992962..160997280-chr2:160998915..161002711,4	K562	blood:
49	chr2:160997618..161000119-chr2:161002297..161003869,2	MCF-7	breast:
50	chr2:161023086..161025481-chr2:161028463..161031210,2	MCF-7	breast:

No data

Variant related genes	Relation type
ITGB6	TF binding region
ENSG00000005483	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000115221	chromatin interactions
ENSG00000228393	chromatin interactions

Extended variants
information (count: 3202 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:3202 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6432594	chr2:160965335-160965336	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs6729540	chr2:160965347-160965348	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs193208378	chr2:160965351-160965352	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73008800	chr2:160965398-160965399	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs116033668	chr2:160965411-160965412	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540467904	chr2:160965421-160965422	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143894951	chr2:160965422-160965423	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199708943	chr2:160965452-160965453	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6758074	chr2:160965483-160965484	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs375595743	chr2:160965513-160965514	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551262288	chr2:160965618-160965619	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116562858	chr2:160965665-160965666	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532782450	chr2:160965683-160965684	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550998427	chr2:160965694-160965695	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566206438	chr2:160965700-160965701	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548388347	chr2:160965719-160965720	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370131868	chr2:160965735-160965736	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148609136	chr2:160965750-160965751	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6747699	chr2:160965781-160965782	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs567460846	chr2:160965799-160965800	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369464335	chr2:160965808-160965809	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537702271	chr2:160965811-160965812	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184718496	chr2:160965817-160965818	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537232403	chr2:160965844-160965845	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575673774	chr2:160965898-160965899	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189046936	chr2:160965936-160965937	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558231695	chr2:160965949-160965950	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573366012	chr2:160965959-160965960	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181391834	chr2:160965978-160965979	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562094076	chr2:160966009-160966010	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117024903	chr2:160966012-160966013	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142116322	chr2:160966035-160966036	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563909286	chr2:160966047-160966048	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532982022	chr2:160966064-160966065	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151158835	chr2:160966074-160966075	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141350039	chr2:160966085-160966086	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185776117	chr2:160966134-160966135	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527352195	chr2:160966144-160966145	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12999707	chr2:160966159-160966160	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567319539	chr2:160966182-160966183	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375384601	chr2:160966190-160966191	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145207750	chr2:160966201-160966202	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs80117332	chr2:160966239-160966240	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571565012	chr2:160966244-160966245	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142308271	chr2:160966289-160966290	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79296968	chr2:160966314-160966315	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573277540	chr2:160966390-160966391	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534011804	chr2:160966392-160966393	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188531785	chr2:160966416-160966417	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574086558	chr2:160966429-160966430	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	18414403	CNVD
Epilepsy	21204806	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:160950800-160967000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:160953200-160970800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:160954600-160970800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:160954600-160993000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr2:160954800-160966200	Weak transcription	Fetal Intestine Small	intestine
6	chr2:160955800-160968800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr2:160956200-160965600	Strong transcription	HMEC	breast
8	chr2:160957000-160970200	Weak transcription	Pancreas	Pancrea
9	chr2:160957400-160981200	Weak transcription	Lung	lung
10	chr2:160959200-161004200	Weak transcription	Gastric	stomach
11	chr2:160959400-160985200	Weak transcription	Esophagus	oesophagus
12	chr2:160959400-161032800	Weak transcription	Psoas Muscle	Psoas
13	chr2:160959800-160965800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:160960000-160966400	Weak transcription	HSMMtube	muscle
15	chr2:160960400-160965600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:160961000-160965600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr2:160962000-160966200	Strong transcription	HSMM	muscle
18	chr2:160962400-160970800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:160962800-160971000	Strong transcription	Placenta Amnion	Placenta Amnion
20	chr2:160963800-160969200	Strong transcription	Skeletal Muscle Male	skeletal muscle
21	chr2:160964200-160993600	Weak transcription	Fetal Muscle Leg	muscle
22	chr2:160964400-160965800	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr2:160964400-160967000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:160964400-160993600	Weak transcription	Fetal Intestine Large	intestine
25	chr2:160964600-160965400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:160964800-160966200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr2:160964800-160970800	Weak transcription	Stomach Mucosa	stomach
28	chr2:160965000-160966400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr2:160965000-160968200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:160965200-160965600	Weak transcription	NHEK	skin
31	chr2:160965200-160968000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:160965400-160966400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:160965400-160966600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:160965600-160966400	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr2:160965600-160967600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:160965600-160968000	Genic enhancers	NHEK	skin
37	chr2:160965600-160969200	Genic enhancers	HMEC	breast
38	chr2:160965800-160966400	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr2:160965800-160967200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr2:160965800-160969600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr2:160966000-160968000	Enhancers	A549	lung
42	chr2:160966200-160967200	Genic enhancers	HSMM	muscle
43	chr2:160966200-160969000	Strong transcription	Fetal Intestine Small	intestine
44	chr2:160966400-160967200	Enhancers	HSMMtube	muscle
45	chr2:160966400-160968600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:160966400-160970600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr2:160966400-160980200	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:160966600-160967000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:160966600-160967200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:160966600-160967600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links