Variant report

Variant	nsv881737
Chromosome Location	chr5:61857577-61877628
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	ATF2	chr5:61870304-61870858	GM12878	blood:	n/a	n/a
2	BACH1	chr5:61865990-61866018	K562	blood:	n/a	n/a
3	BATF	chr5:61870405-61870771	GM12878	blood:	n/a	n/a
4	BATF	chr5:61870477-61870741	GM12878	blood:	n/a	n/a
5	BATF	chr5:61865376-61865608	GM12878	blood:	n/a	chr5:61865577-61865585
6	BCLAF1	chr5:61870371-61870825	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:61872555-61872604	K562	blood:	n/a	n/a
8	CBX3	chr5:61863983-61864320	K562	blood:	n/a	n/a
9	CBX3	chr5:61863976-61864361	K562	blood:	n/a	n/a
10	CCNT2	chr5:61876573-61876767	K562	blood:	n/a	n/a
11	CEBPB	chr5:61861241-61861438	HepG2	liver:	n/a	chr5:61861263-61861274
12	CEBPB	chr5:61861251-61861340	A549	lung:	n/a	chr5:61861263-61861274
13	CTCF	chr5:61858780-61858930	Caco-2	colon:	n/a	chr5:61858899-61858908
14	CTCF	chr5:61858740-61858890	GM12864	blood:	n/a	n/a
15	CTCF	chr5:61858877-61858910	LNCaP	prostate:	n/a	chr5:61858899-61858908
16	CTCF	chr5:61858780-61858930	HEEpiC	esophagus:	n/a	chr5:61858899-61858908
17	CTCF	chr5:61858800-61858950	GM12874	blood:	n/a	chr5:61858899-61858908
18	CTCF	chr5:61858700-61858850	A549	lung:	n/a	n/a
19	CTCF	chr5:61858717-61858948	H1-hESC	embryonic stem cell:	n/a	chr5:61858899-61858908
20	CTCF	chr5:61858800-61858950	HRE	kidney:	n/a	chr5:61858899-61858908
21	CTCF	chr5:61858840-61858990	HEK293	kidney:	n/a	chr5:61858899-61858908
22	CTCF	chr5:61858840-61858990	HCT-116	colon:	n/a	chr5:61858899-61858908
23	CTCF	chr5:61864945-61865031	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr5:61858820-61858970	HepG2	liver:	n/a	chr5:61858899-61858908
25	CTCF	chr5:61858805-61858951	MCF-7	breast:	n/a	chr5:61858899-61858908
26	CTCF	chr5:61858780-61858930	GM12873	blood:	n/a	chr5:61858899-61858908
27	CTCF	chr5:61858820-61858970	HPF	lung:	n/a	chr5:61858899-61858908
28	CTCF	chr5:61858880-61859030	HMEC	breast:	n/a	chr5:61858899-61858908
29	CTCF	chr5:61858760-61858910	GM12873	blood:	n/a	chr5:61858899-61858908
30	CTCF	chr5:61858820-61858970	HRPEpiC	eye:	n/a	chr5:61858899-61858908
31	CTCF	chr5:61858860-61859010	HPAF	blood vessel:	n/a	chr5:61858899-61858908
32	CTCF	chr5:61858760-61858910	RPTEC	kidney:	n/a	chr5:61858899-61858908
33	CTCF	chr5:61861998-61862019	GM13977	blood:	n/a	n/a
34	CTCF	chr5:61858940-61859090	HepG2	liver:	n/a	n/a
35	CTCF	chr5:61858800-61858950	HCT-116	colon:	n/a	chr5:61858899-61858908
36	CTCF	chr5:61858721-61859059	MCF-7	breast:	n/a	chr5:61858899-61858908
37	CTCF	chr5:61858820-61858970	Caco-2	colon:	n/a	chr5:61858899-61858908
38	CTCF	chr5:61858840-61858990	GM12873	blood:	n/a	chr5:61858899-61858908
39	CTCF	chr5:61858813-61858955	MCF-7	breast:	n/a	chr5:61858899-61858908
40	CTCF	chr5:61858820-61858970	AoAF	blood vessel:	n/a	chr5:61858899-61858908
41	CTCF	chr5:61858760-61858910	MCF-7	breast:	n/a	chr5:61858899-61858908
42	CTCF	chr5:61858780-61858930	HMEC	breast:	n/a	chr5:61858899-61858908
43	CTCF	chr5:61858860-61859010	MCF-7	breast:	n/a	chr5:61858899-61858908
44	CTCF	chr5:61858803-61859018	H1-hESC	embryonic stem cell:	n/a	chr5:61858899-61858908
45	CTCF	chr5:61858740-61858890	GM12866	blood:	n/a	n/a
46	CTCF	chr5:61858780-61858930	GM12869	blood:	n/a	chr5:61858899-61858908
47	CTCF	chr5:61858760-61858910	Hela-S3	cervix:	n/a	chr5:61858899-61858908
48	E2F4	chr5:61869234-61869373	MCF10A-Er-Src	breast:	n/a	n/a
49	ELF1	chr5:61874395-61874591	HepG2	liver:	n/a	n/a
50	ELK1	chr5:61874457-61874632	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61876634-61876684	NT2-D1	testis:	n/a
2	chr5:61874017-61874067	Hela-S3	cervix:	n/a
3	chr5:61874017-61874067	T-47D	breast:	n/a
4	chr5:61874017-61874067	ProgFib	skin:	n/a
5	chr5:61876634-61876684	AG04449	skin:	fetal
6	chr5:61876634-61876684	HRCEpiC	kidney:	n/a
7	chr5:61876634-61876684	HRPEpiC	eye:	n/a
8	chr5:61876634-61876684	HepG2	liver:	n/a
9	chr5:61876634-61876684	NH-A	brain:	n/a
10	chr5:61876634-61876684	HCPEpiC	choroid plexus:	n/a
11	chr5:61874017-61874067	HCM	heart:	n/a
12	chr5:61874017-61874067	HRCEpiC	kidney:	n/a
13	chr5:61874017-61874067	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:61876634-61876684	H1-hESC	embryonic stem cell:	embryo
15	chr5:61876634-61876684	SK-N-SH_RA	brain:	n/a
16	chr5:61874017-61874067	NH-A	brain:	n/a
17	chr5:61874017-61874067	K562	blood:	n/a
18	chr5:61874017-61874067	H1-hESC	embryonic stem cell:	embryo
19	chr5:61874017-61874067	NB4	blood:	n/a
20	chr5:61876634-61876684	BE2_C	brain:	n/a
21	chr5:61876634-61876684	HCT-116	colon:	n/a
22	chr5:61876634-61876684	GM19239	blood:	n/a
23	chr5:61876634-61876684	HIPEpiC	eye:	n/a
24	chr5:61876634-61876684	Jurkat	blood:	n/a
25	chr5:61876634-61876684	U87	brain:	n/a
26	chr5:61876634-61876684	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:61874017-61874067	PANC-1	pancreas:	n/a
28	chr5:61876634-61876684	HNPCEpiC	eye:	n/a
29	chr5:61874017-61874067	MCF10A-Er-Src	breast:	n/a
30	chr5:61874017-61874067	Jurkat	blood:	n/a
31	chr5:61876634-61876684	GM12878	blood:	n/a
32	chr5:61874017-61874067	SK-N-SH_RA	brain:	n/a
33	chr5:61874017-61874067	AoSMC	blood vessel:	n/a
34	chr5:61876634-61876684	AG10803	skin:	n/a
35	chr5:61876634-61876684	GM06990	blood:	n/a
36	chr5:61876634-61876684	Hepatocyte	liver:	n/a
37	chr5:61874017-61874067	ovcar-3	ovarian:	n/a
38	chr5:61876634-61876684	Hela-S3	cervix:	n/a
39	chr5:61874017-61874067	NT2-D1	testis:	n/a
40	chr5:61876634-61876684	HUVEC	blood vessel:	n/a
41	chr5:61874017-61874067	LNCaP	prostate:	n/a
42	chr5:61874017-61874067	GM12891	blood:	n/a
43	chr5:61874017-61874067	HEK293	kidney:	embryo
44	chr5:61876634-61876684	K562	blood:	n/a
45	chr5:61874017-61874067	Caco-2	colon:	n/a
46	chr5:61876634-61876684	AoSMC	blood vessel:	n/a
47	chr5:61874017-61874067	HCT-116	colon:	n/a
48	chr5:61874017-61874067	SKMC	muscle:	n/a
49	chr5:61874017-61874067	HUVEC	blood vessel:	n/a
50	chr5:61874017-61874067	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:61875725..61878816-chr5:61880010..61882591,3	MCF-7	breast:
2	chr5:61865017..61866532-chr5:61879181..61880802,2	K562	blood:
3	chr5:61833675..61836577-chr5:61862911..61865153,3	K562	blood:
4	chr5:61875507..61877206-chr5:61878546..61880725,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC70-1	chr5:61874664-61874762	NONHSAT101716
2	lnc-DIMT1-2	chr5:61871778-61872098	NONHSAT101715
3	lnc-DIMT1-1	chr5:61857686-61858043	NONHSAT101714
4	lnc-LRRC70-1	chr5:61876281-61877269	NONHSAT101716
5	lnc-LRRC70-1	chr5:61875228-61875310	NONHSAT101716

Variant related genes	Relation type
ENSG00000241991	TF binding region
LRRC70	TF binding region
ENSG00000240436	TF binding region
IPO11	TF binding region
ENSG00000241991	CpG island
LRRC70	CpG island
ENSG00000240436	CpG island
IPO11	CpG island

Extended variants
information (count: 688 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs32163	chr5:61857577-61857578	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559607884	chr5:61857605-61857606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536747536	chr5:61857626-61857627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188228257	chr5:61857634-61857635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372376261	chr5:61857643-61857644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572820752	chr5:61857705-61857706	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs545078980	chr5:61857789-61857790	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs182077332	chr5:61857820-61857821	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs200538944	chr5:61857825-61857826	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs576003785	chr5:61857876-61857877	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs139469966	chr5:61857911-61857912	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs564652776	chr5:61857959-61857960	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs533490956	chr5:61857965-61857966	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs547092981	chr5:61858015-61858016	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs560350096	chr5:61858047-61858048	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs34689768	chr5:61858076-61858077	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs32162	chr5:61858163-61858164	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs144155449	chr5:61858172-61858173	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs568061520	chr5:61858209-61858210	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536939064	chr5:61858211-61858212	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs35095981	chr5:61858238-61858239	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147975880	chr5:61858257-61858258	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367735370	chr5:61858284-61858285	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570293041	chr5:61858305-61858306	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539231169	chr5:61858306-61858307	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569824043	chr5:61858330-61858331	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553049368	chr5:61858345-61858346	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184872549	chr5:61858359-61858360	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140183618	chr5:61858397-61858398	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs189305798	chr5:61858496-61858497	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576039835	chr5:61858563-61858564	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537212520	chr5:61858595-61858596	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375089243	chr5:61858628-61858629	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs564742106	chr5:61858645-61858646	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs578226563	chr5:61858656-61858657	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs13174978	chr5:61858661-61858662	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560637116	chr5:61858677-61858678	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs7722527	chr5:61858728-61858729	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543050711	chr5:61858833-61858834	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs562528152	chr5:61858839-61858840	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530741653	chr5:61858887-61858888	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550485571	chr5:61858921-61858922	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs570382287	chr5:61858927-61858928	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs186619620	chr5:61858963-61858964	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs546434011	chr5:61858989-61858990	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566600626	chr5:61858991-61858992	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs189894810	chr5:61858992-61858993	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs181214299	chr5:61858996-61858997	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs568889313	chr5:61859011-61859012	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs74636445	chr5:61859082-61859083	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61739200-61862800	Weak transcription	Brain Substantia Nigra	brain
2	chr5:61748000-61862800	Weak transcription	Right Ventricle	heart
3	chr5:61758800-61890000	Weak transcription	Small Intestine	intestine
4	chr5:61764000-61858200	Weak transcription	Placenta	Placenta
5	chr5:61764200-61895800	Weak transcription	Pancreas	Pancrea
6	chr5:61771200-61864800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:61771400-61863000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:61781600-61867600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr5:61787400-61866800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr5:61793600-61905000	Weak transcription	NHEK	skin
11	chr5:61796600-61866600	Weak transcription	Osteobl	bone
12	chr5:61796800-61899000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr5:61797000-61861200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:61802600-61889000	Weak transcription	NH-A	brain
15	chr5:61803000-61904400	Weak transcription	Fetal Kidney	kidney
16	chr5:61803200-61875000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr5:61803400-61863600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:61804400-61865200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr5:61806800-61863400	Weak transcription	Lung	lung
20	chr5:61812200-61865200	Weak transcription	HUVEC	blood vessel
21	chr5:61815000-61861400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:61815200-61890600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr5:61816000-61857800	Weak transcription	Fetal Stomach	stomach
24	chr5:61816200-61862200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr5:61819200-61860400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:61819800-61861600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:61821400-61863400	Weak transcription	Aorta	Aorta
28	chr5:61827200-61858200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr5:61827200-61861200	Weak transcription	Liver	Liver
30	chr5:61827200-61883600	Weak transcription	HepG2	liver
31	chr5:61827400-61862800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr5:61827400-61899200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr5:61828200-61861600	Weak transcription	Brain Hippocampus Middle	brain
34	chr5:61828200-61862800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr5:61828200-61864400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr5:61828200-61886800	Weak transcription	Duodenum Mucosa	Duodenum
37	chr5:61828600-61858000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr5:61828600-61861600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:61831400-61871800	Weak transcription	Psoas Muscle	Psoas
40	chr5:61834200-61861400	Weak transcription	GM12878-XiMat	blood
41	chr5:61834800-61858200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr5:61834800-61858200	Weak transcription	Fetal Brain Female	brain
43	chr5:61834800-61861000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr5:61834800-61861600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr5:61834800-61864600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr5:61834800-61899200	Weak transcription	Esophagus	oesophagus
47	chr5:61835200-61857800	Weak transcription	Left Ventricle	heart
48	chr5:61835200-61861600	Weak transcription	Fetal Lung	lung
49	chr5:61835200-61861600	Weak transcription	Fetal Muscle Trunk	muscle
50	chr5:61836200-61861600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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