Variant report

Variant	nsv897067
Chromosome Location	chr11:23777459-23861558
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:202)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:23808741-23808892	HepG2	liver:	n/a	n/a
2	BRCA1	chr11:23791141-23791164	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr11:23820809-23821124	HepG2	liver:	n/a	chr11:23821104-23821117
4	CEBPB	chr11:23829111-23829319	K562	blood:	n/a	chr11:23829233-23829244
5	CEBPB	chr11:23829094-23829349	A549	lung:	n/a	chr11:23829233-23829244
6	CEBPB	chr11:23844303-23844514	HepG2	liver:	n/a	chr11:23844394-23844405
7	CEBPB	chr11:23820772-23821109	A549	lung:	n/a	n/a
8	CEBPB	chr11:23794359-23794613	HepG2	liver:	n/a	chr11:23794482-23794495 chr11:23794482-23794493
9	CEBPB	chr11:23808790-23808947	HepG2	liver:	n/a	chr11:23808906-23808917
10	CEBPB	chr11:23777366-23777662	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:23829075-23829384	HepG2	liver:	n/a	chr11:23829233-23829244
12	CEBPB	chr11:23829064-23829390	IMR90	lung:	n/a	chr11:23829233-23829244
13	CEBPB	chr11:23844250-23844479	IMR90	lung:	n/a	chr11:23844394-23844405
14	CEBPB	chr11:23777380-23777595	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:23820766-23821130	IMR90	lung:	n/a	chr11:23821104-23821117
16	CHD1	chr11:23789645-23789701	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr11:23855960-23856110	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr11:23855952-23856153	MCF-7	breast:	n/a	n/a
19	CTCF	chr11:23855920-23856070	MCF-7	breast:	n/a	n/a
20	CTCF	chr11:23855960-23856110	HCFaa	heart:	n/a	n/a
21	CTCF	chr11:23855936-23856164	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:23855960-23856110	HPF	lung:	n/a	n/a
23	CTCF	chr11:23855960-23856110	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr11:23855860-23856010	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr11:23856012-23856107	ProgFib	skin:	n/a	n/a
26	CTCF	chr11:23855960-23856110	HRE	kidney:	n/a	n/a
27	CTCF	chr11:23855960-23856110	HMF	breast:	n/a	n/a
28	CTCF	chr11:23849268-23849376	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr11:23855989-23856128	Gliobla	brain:	n/a	n/a
30	CTCF	chr11:23855968-23856123	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:23856139-23856154	Fibrobl	skin:	n/a	n/a
32	CTCF	chr11:23855967-23856138	Fibrobl	skin:	n/a	n/a
33	CTCF	chr11:23855960-23856110	Caco-2	colon:	n/a	n/a
34	CTCF	chr11:23849360-23849510	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:23855940-23856090	AG09319	gingival:	n/a	n/a
36	CTCF	chr11:23827236-23827314	ProgFib	skin:	n/a	n/a
37	CTCF	chr11:23855960-23856110	AG04449	skin:	n/a	n/a
38	CTCF	chr11:23855940-23856090	HMF	breast:	n/a	n/a
39	CTCF	chr11:23855980-23856130	HMEC	breast:	n/a	n/a
40	CTCF	chr11:23855920-23856070	AG09309	skin:	n/a	n/a
41	CTCF	chr11:23856000-23856150	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr11:23855956-23856145	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr11:23855900-23856050	HVMF	connective:	n/a	n/a
44	CTCF	chr11:23855940-23856090	HMEC	breast:	n/a	n/a
45	CTCF	chr11:23855880-23856030	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr11:23855920-23856070	BJ	skin:	n/a	n/a
47	CTCF	chr11:23855980-23856130	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr11:23855960-23856110	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr11:23855926-23856203	IMR90	lung:	n/a	n/a
50	CTCF	chr11:23855960-23856110	AG10803	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:23811425-23811475	HIPEpiC	eye:	n/a
2	chr11:23811425-23811475	HRPEpiC	eye:	n/a
3	chr11:23811425-23811475	SK-N-SH_RA	brain:	n/a
4	chr11:23811425-23811475	AG09309	skin:	n/a
5	chr11:23811425-23811475	HMEC	breast:	n/a
6	chr11:23811425-23811475	NHBE	bronchial:	n/a
7	chr11:23811425-23811475	NB4	blood:	n/a
8	chr11:23811425-23811475	HNPCEpiC	eye:	n/a
9	chr11:23811425-23811475	MCF10A-Er-Src	breast:	n/a
10	chr11:23811425-23811475	BJ	skin:	n/a
11	chr11:23811425-23811475	PANC-1	pancreas:	n/a
12	chr11:23811425-23811475	GM19239	blood:	n/a
13	chr11:23811425-23811475	SKMC	muscle:	n/a
14	chr11:23811425-23811475	HL-60	blood:	n/a
15	chr11:23811425-23811475	HepG2	liver:	n/a
16	chr11:23811425-23811475	HCT-116	colon:	n/a
17	chr11:23811425-23811475	Hela-S3	cervix:	n/a
18	chr11:23811425-23811475	U87	brain:	n/a
19	chr11:23811425-23811475	HRCEpiC	kidney:	n/a
20	chr11:23811425-23811475	GM06990	blood:	n/a
21	chr11:23811425-23811475	HEEpiC	esophagus:	n/a
22	chr11:23811425-23811475	HCM	heart:	n/a
23	chr11:23811425-23811475	A549	lung:	n/a
24	chr11:23811425-23811475	Jurkat	blood:	n/a
25	chr11:23811425-23811475	AoSMC	blood vessel:	n/a
26	chr11:23811425-23811475	HCF	heart:	n/a
27	chr11:23811425-23811475	ovcar-3	ovarian:	n/a
28	chr11:23811425-23811475	SAEC	small airway:	n/a
29	chr11:23811425-23811475	HAEpiC	amniotic membrane:	n/a
30	chr11:23811425-23811475	AG10803	skin:	n/a
31	chr11:23811425-23811475	NHDF-neo	bronchial:	n/a
32	chr11:23811425-23811475	PFSK-1	brain:	n/a
33	chr11:23811425-23811475	LNCaP	prostate:	n/a
34	chr11:23811425-23811475	T-47D	breast:	n/a
35	chr11:23811425-23811475	AG04450	lung:	fetal
36	chr11:23811425-23811475	GM12891	blood:	n/a
37	chr11:23811425-23811475	GM12878	blood:	n/a
38	chr11:23811425-23811475	CMK	blood:	n/a
39	chr11:23811425-23811475	HRE	kidney:	n/a
40	chr11:23811425-23811475	H1-hESC	embryonic stem cell:	embryo
41	chr11:23811425-23811475	SK-N-MC	brain:	n/a
42	chr11:23811425-23811475	HCPEpiC	choroid plexus:	n/a
43	chr11:23811425-23811475	ProgFib	skin:	n/a
44	chr11:23811425-23811475	HUVEC	blood vessel:	n/a
45	chr11:23811425-23811475	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:23811425-23811475	MCF-7	breast:	n/a
47	chr11:23811425-23811475	IMR90	lung:	fetal
48	chr11:23811425-23811475	RPTEC	kidney:	n/a
49	chr11:23811425-23811475	NH-A	brain:	n/a
50	chr11:23811425-23811475	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:23798376..23799116-chr5:32449587..32450235,2	MCF-7	breast:
2	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:
3	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LUZP2-1	chr11:23818254-23818516	ENSG00000255193
2	lnc-LUZP2-1	chr11:23816369-23816430	ENSG00000255193
3	lnc-RP11-17A1.2.1-2	chr11:23802334-23802418	ENSG00000254861
4	lnc-RP11-17A1.2.1-2	chr11:23782899-23783176	XLOC_009394
5	lnc-RP11-17A1.2.1-5	chr11:23818256-23819005	NONHSAT018430
6	lnc-RP11-17A1.2.1-2	chr11:23826000-23826222	XLOC_009395
7	lnc-RP11-17A1.2.1-2	chr11:23826025-23826144	ENSG00000254861
8	lnc-RP11-17A1.2.1-2	chr11:23782876-23783176	ENSG00000254861
9	lnc-RP11-17A1.2.1-2	chr11:23789323-23789362	XLOC_009394
10	lnc-RP11-17A1.2.1-2	chr11:23829736-23829778	XLOC_009395
11	lnc-RP11-17A1.2.1-5	chr11:23817463-23817487	NONHSAT018430

No data

Variant related genes	Relation type
ENSG00000254861	TF binding region
ENSG00000254861	CpG island

Extended variants
information (count: 2159 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2159 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4317983	chr11:23777459-23777460	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538428310	chr11:23777478-23777479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185298483	chr11:23777537-23777538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142118545	chr11:23777564-23777565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555266182	chr11:23777591-23777592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574883034	chr11:23777592-23777593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190061205	chr11:23777596-23777597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115877560	chr11:23777599-23777600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182690126	chr11:23777603-23777604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34573506	chr11:23777605-23777606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369353705	chr11:23777607-23777608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs151156862	chr11:23777608-23777609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529768437	chr11:23777665-23777666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187770821	chr11:23777682-23777683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565758294	chr11:23777701-23777702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576804724	chr11:23777712-23777713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533109418	chr11:23777718-23777719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542482982	chr11:23777722-23777723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562094078	chr11:23777734-23777735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527404397	chr11:23777737-23777738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11821406	chr11:23777765-23777766	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs192466839	chr11:23777789-23777790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114671097	chr11:23777821-23777822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549365429	chr11:23777835-23777836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375706342	chr11:23777848-23777849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529108470	chr11:23777864-23777865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549161819	chr11:23777878-23777879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551469405	chr11:23777905-23777906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11828544	chr11:23777932-23777933	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs76299983	chr11:23778031-23778032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183928971	chr11:23778032-23778033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77357961	chr11:23778037-23778038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554060250	chr11:23778133-23778134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188868910	chr11:23778140-23778141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111330881	chr11:23778141-23778142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs61876074	chr11:23778172-23778173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs556587793	chr11:23778201-23778202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576812097	chr11:23778214-23778215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542130496	chr11:23778250-23778251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150465722	chr11:23778274-23778275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370502326	chr11:23778275-23778276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12269859	chr11:23778284-23778285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs541593068	chr11:23778285-23778286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564075082	chr11:23778293-23778294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532856999	chr11:23778311-23778312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543026078	chr11:23778316-23778317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74566312	chr11:23778334-23778335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562894595	chr11:23778336-23778337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529169744	chr11:23778362-23778363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191975820	chr11:23778403-23778404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23772400-23782400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:23776600-23777800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:23777000-23778200	Enhancers	Adipose Nuclei	Adipose
4	chr11:23778600-23779000	Enhancers	Fetal Intestine Large	intestine
5	chr11:23780800-23781400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:23781200-23781400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr11:23781400-23785400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:23781400-23787200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr11:23782000-23783200	Enhancers	Fetal Lung	lung
10	chr11:23782400-23783200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:23785400-23789000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:23786200-23786400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr11:23787000-23788200	Enhancers	Placenta Amnion	Placenta Amnion
14	chr11:23787200-23788000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:23787200-23788000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr11:23787200-23788200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr11:23789200-23792000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:23790200-23791200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr11:23790400-23791800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:23792600-23794200	Enhancers	Fetal Stomach	stomach
21	chr11:23792800-23794200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr11:23794200-23795200	Weak transcription	Fetal Stomach	stomach
23	chr11:23795200-23795400	Enhancers	Fetal Stomach	stomach
24	chr11:23798600-23799200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:23799200-23803200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr11:23799600-23802400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:23800400-23802000	Enhancers	NH-A	brain
28	chr11:23800600-23802600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:23800800-23801200	Enhancers	HSMM	muscle
30	chr11:23801200-23811000	Weak transcription	HSMM	muscle
31	chr11:23803200-23803600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr11:23803600-23804600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:23804600-23806800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:23805200-23806400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr11:23805800-23806200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:23806200-23811200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:23806400-23806600	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr11:23806400-23807000	Enhancers	HepG2	liver
39	chr11:23806600-23806800	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr11:23806800-23808200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr11:23806800-23808200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr11:23807000-23808000	Weak transcription	HepG2	liver
43	chr11:23807000-23809000	Enhancers	Fetal Intestine Small	intestine
44	chr11:23807400-23808600	Enhancers	Fetal Lung	lung
45	chr11:23807800-23809400	Enhancers	Stomach Mucosa	stomach
46	chr11:23808000-23809400	Enhancers	Fetal Intestine Large	intestine
47	chr11:23808000-23809600	Enhancers	HepG2	liver
48	chr11:23808200-23809000	Enhancers	Gastric	stomach
49	chr11:23808200-23809000	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr11:23808200-23809600	Enhancers	Rectal Mucosa Donor 31	rectum

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