Variant report

Variant	nsv874663
Chromosome Location	chr2:96345518-96459313
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	ARID3A	chr2:96394384-96394976	HepG2	liver:	n/a	n/a
2	BATF	chr2:96401104-96401456	GM12878	blood:	n/a	n/a
3	BATF	chr2:96389629-96389835	GM12878	blood:	n/a	n/a
4	BATF	chr2:96389586-96389891	GM12878	blood:	n/a	n/a
5	BATF	chr2:96373017-96373229	GM12878	blood:	n/a	chr2:96373152-96373163
6	BATF	chr2:96373042-96373284	GM12878	blood:	n/a	chr2:96373152-96373163
7	BCL11A	chr2:96401015-96401259	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:96401104-96401290	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:96442951-96443157	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:96394763-96394892	GM12878	blood:	n/a	n/a
11	CBX3	chr2:96432533-96432779	K562	blood:	n/a	n/a
12	CEBPB	chr2:96352306-96352520	A549	lung:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
13	CEBPB	chr2:96391404-96391735	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:96394271-96395330	HepG2	liver:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
15	CEBPB	chr2:96352290-96352412	HepG2	liver:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
16	CEBPB	chr2:96352308-96352398	Hela-S3	cervix:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
17	CEBPB	chr2:96394709-96395335	K562	blood:	n/a	n/a
18	CEBPB	chr2:96394316-96394473	K562	blood:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
19	CEBPB	chr2:96426884-96427208	Hela-S3	cervix:	n/a	chr2:96427040-96427051
20	CEBPB	chr2:96426939-96427088	HepG2	liver:	n/a	chr2:96427040-96427051
21	CEBPB	chr2:96352152-96352528	IMR90	lung:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
22	CEBPB	chr2:96394654-96395269	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:96353649-96353979	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:96426902-96427182	MCF-7	breast:	n/a	chr2:96427040-96427051
25	CEBPB	chr2:96394342-96395320	A549	lung:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
26	CEBPB	chr2:96426837-96427246	IMR90	lung:	n/a	chr2:96427040-96427051
27	CEBPB	chr2:96361449-96361668	K562	blood:	n/a	n/a
28	CEBPB	chr2:96394289-96395327	IMR90	lung:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
29	CEBPB	chr2:96394684-96394919	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:96352196-96352515	A549	lung:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
31	CEBPB	chr2:96352310-96352556	MCF-7	breast:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
32	CTCF	chr2:96441010-96441186	GM10266	blood:	n/a	chr2:96441089-96441107
33	CTCF	chr2:96456017-96456248	K562	blood:	n/a	n/a
34	CTCF	chr2:96394635-96395050	K562	blood:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
35	CTCF	chr2:96394680-96394830	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr2:96429847-96429890	Gliobla	brain:	n/a	n/a
37	CTCF	chr2:96417404-96417481	LNCaP	prostate:	n/a	n/a
38	CTCF	chr2:96455998-96456057	Fibrobl	skin:	n/a	n/a
39	CTCF	chr2:96422632-96422738	Lung_OC	lung:	n/a	n/a
40	CTCF	chr2:96429789-96429903	GM13976	blood:	n/a	chr2:96429822-96429840
41	CTCF	chr2:96394740-96394890	HFF-Myc	foreskin:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
42	CTCF	chr2:96394759-96394962	GM13976	blood:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
43	CTCF	chr2:96394758-96394966	GM10248	blood:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
44	CTCF	chr2:96429786-96429910	K562	blood:	n/a	chr2:96429822-96429840
45	CTCF	chr2:96455956-96456196	K562	blood:	n/a	n/a
46	CTCF	chr2:96440948-96441108	MCF-7	breast:	n/a	chr2:96441089-96441107
47	CTCF	chr2:96394740-96394890	HMEC	breast:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
48	CTCF	chr2:96394980-96395130	GM12801	blood:	n/a	n/a
49	CTCF	chr2:96394758-96394979	GM10266	blood:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
50	CTCF	chr2:96394780-96394930	RPTEC	kidney:	n/a	chr2:96394849-96394870 chr2:96394854-96394872

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96458247-96458297	HepG2	liver:	n/a
2	chr2:96427173-96427223	AoSMC	blood vessel:	n/a
3	chr2:96458247-96458297	Jurkat	blood:	n/a
4	chr2:96348691-96348741	AoSMC	blood vessel:	n/a
5	chr2:96427173-96427223	RPTEC	kidney:	n/a
6	chr2:96427173-96427223	Jurkat	blood:	n/a
7	chr2:96348691-96348741	HRPEpiC	eye:	n/a
8	chr2:96348691-96348741	ovcar-3	ovarian:	n/a
9	chr2:96458247-96458297	NHDF-neo	bronchial:	n/a
10	chr2:96427173-96427223	NT2-D1	testis:	n/a
11	chr2:96348691-96348741	HRCEpiC	kidney:	n/a
12	chr2:96427173-96427223	Caco-2	colon:	n/a
13	chr2:96458247-96458297	HRCEpiC	kidney:	n/a
14	chr2:96458247-96458297	GM12892	blood:	n/a
15	chr2:96348691-96348741	HCT-116	colon:	n/a
16	chr2:96348691-96348741	HNPCEpiC	eye:	n/a
17	chr2:96427173-96427223	HCT-116	colon:	n/a
18	chr2:96427173-96427223	PFSK-1	brain:	n/a
19	chr2:96348691-96348741	NB4	blood:	n/a
20	chr2:96427173-96427223	PANC-1	pancreas:	n/a
21	chr2:96348691-96348741	BJ	skin:	n/a
22	chr2:96348691-96348741	ProgFib	skin:	n/a
23	chr2:96427173-96427223	SK-N-MC	brain:	n/a
24	chr2:96458247-96458297	MCF10A-Er-Src	breast:	n/a
25	chr2:96348691-96348741	HCM	heart:	n/a
26	chr2:96427173-96427223	HL-60	blood:	n/a
27	chr2:96348691-96348741	SK-N-MC	brain:	n/a
28	chr2:96348691-96348741	HMEC	breast:	n/a
29	chr2:96458247-96458297	HL-60	blood:	n/a
30	chr2:96348691-96348741	Hepatocyte	liver:	n/a
31	chr2:96348691-96348741	SKMC	muscle:	n/a
32	chr2:96427173-96427223	HRE	kidney:	n/a
33	chr2:96458247-96458297	HCPEpiC	choroid plexus:	n/a
34	chr2:96348691-96348741	HEK293	kidney:	embryo
35	chr2:96458247-96458297	HNPCEpiC	eye:	n/a
36	chr2:96427173-96427223	HUVEC	blood vessel:	n/a
37	chr2:96427173-96427223	PrEC	prostate:	n/a
38	chr2:96427173-96427223	U87	brain:	n/a
39	chr2:96348691-96348741	AG04450	lung:	fetal
40	chr2:96427173-96427223	MCF-7	breast:	n/a
41	chr2:96348691-96348741	RPTEC	kidney:	n/a
42	chr2:96427173-96427223	NB4	blood:	n/a
43	chr2:96427173-96427223	AG10803	skin:	n/a
44	chr2:96458247-96458297	GM12878	blood:	n/a
45	chr2:96348691-96348741	NHBE	bronchial:	n/a
46	chr2:96348691-96348741	A549	lung:	n/a
47	chr2:96458247-96458297	K562	blood:	n/a
48	chr2:96348691-96348741	T-47D	breast:	n/a
49	chr2:96458247-96458297	HEEpiC	esophagus:	n/a
50	chr2:96348691-96348741	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96054639..96055198-chr2:96394784..96395584,2	K562	blood:
2	chr2:96406055..96406842-chr2:114139694..114140465,2	MCF-7	breast:
3	chr2:96054886..96055732-chr2:96394556..96395496,2	MCF-7	breast:
4	chr2:96054634..96055511-chr2:96394406..96395211,2	MCF-7	breast:
5	chr2:96362570..96365117-chr2:96367359..96369981,2	MCF-7	breast:
6	chr2:96058513..96059040-chr2:96394487..96395166,2	MCF-7	breast:
7	chr2:96362570..96365117-chr2:96367359..96369981,2	MCF-7	breast:
8	chr2:96011050..96011912-chr2:96394384..96395342,2	MCF-7	breast:
9	chr2:96079865..96080377-chr2:96394455..96395330,2	K562	blood:
10	chr13:60970490..60971024-chr2:96378837..96379342,2	NB4	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36C-2	chr2:96383793-96384234	XLOC_002206
2	lnc-ANKRD36C-2	chr2:96379286-96379320	XLOC_002206

Variant related genes	Relation type
ENSG00000237510	TF binding region
ENSG00000237510	CpG island
ENSG00000083544	chromatin interactions
ENSG00000248821	chromatin interactions

Extended variants
information (count: 2212 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2212 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11164049	chr2:96345518-96345519	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536165186	chr2:96345543-96345544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373725888	chr2:96345568-96345569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180701577	chr2:96345569-96345570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185274571	chr2:96345590-96345591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190961015	chr2:96345597-96345598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367832326	chr2:96345677-96345678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553341676	chr2:96345680-96345681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576878732	chr2:96345761-96345762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114320716	chr2:96345788-96345789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562723067	chr2:96345822-96345823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141037774	chr2:96345915-96345916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182291234	chr2:96346066-96346067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559936361	chr2:96346094-96346095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562010857	chr2:96346104-96346105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533343850	chr2:96346132-96346133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527575176	chr2:96346133-96346134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547823907	chr2:96346148-96346149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187359426	chr2:96346149-96346150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191700616	chr2:96346155-96346156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549974860	chr2:96346172-96346173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570082367	chr2:96346239-96346240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531209012	chr2:96346243-96346244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535700756	chr2:96346393-96346394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549160739	chr2:96346454-96346455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549414740	chr2:96346479-96346480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566069855	chr2:96346505-96346506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371996597	chr2:96346524-96346525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182961102	chr2:96346573-96346574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146715208	chr2:96346595-96346596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576735000	chr2:96346598-96346599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534946950	chr2:96346638-96346639	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552646925	chr2:96346639-96346640	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186837805	chr2:96346660-96346661	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190153035	chr2:96346666-96346667	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542087064	chr2:96346672-96346673	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561825274	chr2:96346675-96346676	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572375231	chr2:96346743-96346744	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541306049	chr2:96346761-96346762	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564522344	chr2:96346776-96346777	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533208845	chr2:96346835-96346836	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550129835	chr2:96346917-96346918	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571035303	chr2:96346918-96346919	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563675825	chr2:96346931-96346932	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529335103	chr2:96346932-96346933	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140396566	chr2:96346940-96346941	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs5022421	chr2:96346977-96346978	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565886994	chr2:96346983-96346984	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535006146	chr2:96346993-96346994	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537120110	chr2:96347104-96347105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96343600-96347600	Weak transcription	Liver	Liver
2	chr2:96344000-96347600	Weak transcription	Fetal Intestine Small	intestine
3	chr2:96344800-96345600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:96345000-96345800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:96345200-96345800	Enhancers	NHEK	skin
6	chr2:96345400-96345600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:96345400-96345600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:96345400-96347800	Weak transcription	HMEC	breast
9	chr2:96345400-96348000	Weak transcription	Esophagus	oesophagus
10	chr2:96345600-96345800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:96345600-96347600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:96345800-96347600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:96345800-96347600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:96345800-96347800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:96345800-96347800	Weak transcription	NHEK	skin
16	chr2:96346400-96348000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr2:96346600-96346800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
18	chr2:96346800-96347000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:96346800-96347000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:96346800-96347000	Enhancers	Spleen	Spleen
21	chr2:96347000-96347600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:96347000-96348000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:96347000-96348000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:96347000-96348000	Weak transcription	Spleen	Spleen
25	chr2:96347000-96348000	Enhancers	NHDF-Ad	bronchial
26	chr2:96347200-96348000	Enhancers	NHLF	lung
27	chr2:96347400-96347800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr2:96347400-96347800	Enhancers	Brain Cingulate Gyrus	brain
29	chr2:96347400-96348000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:96347400-96348000	Enhancers	Fetal Lung	lung
31	chr2:96347400-96348000	Enhancers	Fetal Muscle Trunk	muscle
32	chr2:96347400-96348200	Enhancers	Fetal Heart	heart
33	chr2:96347600-96347800	Enhancers	Brain Hippocampus Middle	brain
34	chr2:96347600-96347800	Enhancers	Stomach Smooth Muscle	stomach
35	chr2:96347600-96348000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:96347600-96348000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr2:96347600-96348000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr2:96347600-96348000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:96347600-96348000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr2:96347600-96348000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr2:96347600-96348000	Enhancers	Adipose Nuclei	Adipose
42	chr2:96347600-96348000	Enhancers	Liver	Liver
43	chr2:96347600-96348000	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr2:96347600-96348000	Enhancers	Fetal Intestine Large	intestine
45	chr2:96347600-96348000	Enhancers	Fetal Intestine Small	intestine
46	chr2:96347600-96348000	Enhancers	Fetal Muscle Leg	muscle
47	chr2:96347600-96348000	Enhancers	Fetal Stomach	stomach
48	chr2:96347600-96348000	Enhancers	Fetal Thymus	thymus
49	chr2:96347600-96348000	Enhancers	NH-A	brain
50	chr2:96347600-96348000	Enhancers	Osteobl	bone

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