Variant report

Variant	esv1831688
Chromosome Location	chr11:119346590-119387267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:68)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:119368363..119370188-chr11:119375309..119377748,2	K562	blood:
2	chr11:119351120..119353345-chr11:119978719..119981156,2	MCF-7	breast:
3	chr11:119227301..119229062-chr11:119346080..119347995,2	K562	blood:
4	chr11:119352713..119354484-chr11:119363085..119365615,2	K562	blood:
5	chr11:119353955..119356494-chr11:119359612..119362116,3	K562	blood:
6	chr11:119355740..119356652-chr11:119404341..119405194,3	MCF-7	breast:
7	chr11:119352030..119353608-chr11:119494198..119496133,2	K562	blood:
8	chr11:118964673..118967304-chr11:119349058..119352266,5	MCF-7	breast:
9	chr11:119367569..119369775-chr11:119371504..119373804,2	K562	blood:
10	chr11:119362139..119363168-chr11:119404231..119405012,3	K562	blood:
11	chr11:119367569..119369775-chr11:119371504..119373804,2	K562	blood:
12	chr11:119349564..119353198-chr11:119356319..119358488,3	MCF-7	breast:
13	chr11:118954117..118956567-chr11:119362558..119364411,2	MCF-7	breast:
14	chr11:119351803..119352733-chr11:119403995..119405378,11	K562	blood:
15	chr11:119227275..119227862-chr11:119350194..119350776,2	MCF-7	breast:
16	chr11:119349748..119352614-chr11:119597738..119600036,2	MCF-7	breast:
17	chr11:119351964..119353537-chr11:119977212..119979558,2	MCF-7	breast:
18	chr11:119373107..119376972-chr11:119379508..119382925,3	K562	blood:
19	chr11:119370568..119373070-chr11:119375931..119378638,2	MCF-7	breast:
20	chr11:119351776..119352636-chr11:119404331..119405333,6	MCF-7	breast:
21	chr11:119227078..119227608-chr11:119350334..119351290,2	K562	blood:
22	chr11:119381448..119383386-chr11:119384620..119386912,2	K562	blood:
23	chr11:119373107..119376972-chr11:119379508..119382925,3	K562	blood:
24	chr11:119362733..119364322-chr11:119367518..119370066,2	K562	blood:
25	chr11:119382501..119384406-chr11:119454171..119456496,2	K562	blood:
26	chr11:119344891..119347210-chr11:119349502..119351029,2	MCF-7	breast:
27	chr11:118900110..118901741-chr11:119371227..119372995,2	MCF-7	breast:
28	chr11:119247859..119250611-chr11:119367940..119370317,2	K562	blood:
29	chr11:119352209..119352749-chr11:120039546..120040470,2	K562	blood:
30	chr11:119210108..119212084-chr11:119349983..119352434,2	K562	blood:
31	chr11:119351756..119352703-chr11:119978610..119979156,4	K562	blood:
32	chr11:118964686..118967059-chr11:119373256..119374804,2	MCF-7	breast:
33	chr11:118922015..118923746-chr11:119354928..119356715,2	MCF-7	breast:
34	chr11:118899935..118902641-chr11:119356876..119358839,2	MCF-7	breast:
35	chr11:119368363..119370188-chr11:119375309..119377748,2	K562	blood:
36	chr11:119362108..119363327-chr11:119404415..119405170,4	MCF-7	breast:
37	chr11:119370568..119373070-chr11:119375931..119378638,2	MCF-7	breast:
38	chr11:119252341..119254091-chr11:119344729..119346901,2	K562	blood:
39	chr11:119191259..119193835-chr11:119343897..119346665,2	K562	blood:
40	chr11:119381621..119384153-chr11:119388381..119390461,2	K562	blood:
41	chr11:119371118..119373114-chr11:119374717..119376631,2	K562	blood:
42	chr11:119352054..119354278-chr11:119356134..119357864,2	K562	blood:
43	chr11:119362733..119364322-chr11:119367518..119370066,2	K562	blood:
44	chr11:119187492..119189176-chr11:119345752..119348208,2	K562	blood:
45	chr11:119351812..119352603-chr11:119494941..119495456,2	K562	blood:
46	chr11:119351963..119352520-chr11:119537162..119537779,2	MCF-7	breast:
47	chr11:119352713..119354484-chr11:119363085..119365615,2	K562	blood:
48	chr11:119367505..119370039-chr11:119404358..119405876,2	MCF-7	breast:
49	chr11:119341330..119343728-chr11:119345375..119347336,2	MCF-7	breast:
50	chr11:118964732..118966540-chr11:119350138..119352269,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THY1-3	chr11:119368596-119368638	l_553_chr11:119363873-119368638_testes
2	lnc-THY1-3	chr11:119364510-119365375	l_553_chr11:119363873-119368638_testes
3	lnc-RP11-305N23.1.1-1	chr11:119381020-119381191	ENSG00000245248.3
4	lnc-RP11-305N23.1.1-1	chr11:119369261-119369944	NR_034160
5	lnc-RP11-305N23.1.1-1	chr11:119379825-119379936	ENSG00000245248.3
6	lnc-RP11-305N23.1.1-1	chr11:119369261-119371306	ENSG00000245248.3
7	lnc-RP11-305N23.1.1-1	chr11:119369261-119369944	ENSG00000245248.3
8	lnc-THY1-3	chr11:119363874-119364146	l_553_chr11:119363873-119368638_testes
9	lnc-THY1-3	chr11:119370513-119370622	l_553_chr11:119363873-119368638_testes

No data

Variant related genes	Relation type
ENSG00000137700	chromatin interactions
ENSG00000245248	chromatin interactions
ENSG00000254854	chromatin interactions
ENSG00000256269	chromatin interactions
ENSG00000176984	chromatin interactions
ENSG00000223953	chromatin interactions
ENSG00000076706	chromatin interactions
ENSG00000110400	chromatin interactions
ENSG00000188486	chromatin interactions
ENSG00000036672	chromatin interactions

Extended variants
information (count: 1624 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1624 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558342410	chr11:119346596-119346597	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs72995116	chr11:119346665-119346666	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs12292807	chr11:119346693-119346694	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs563032071	chr11:119346731-119346732	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs654776	chr11:119346737-119346738	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542255227	chr11:119346773-119346774	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs539990304	chr11:119346815-119346816	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs75700146	chr11:119346839-119346840	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs138537884	chr11:119346855-119346856	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs141613999	chr11:119346857-119346858	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs552768665	chr11:119346861-119346862	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs146225674	chr11:119346917-119346918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373754353	chr11:119346920-119346921	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs139145496	chr11:119346921-119346922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550388048	chr11:119346925-119346926	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149918371	chr11:119346941-119346942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368499413	chr11:119346965-119346966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191019827	chr11:119346976-119346977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368462384	chr11:119346984-119346985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs647369	chr11:119347074-119347075	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs72995125	chr11:119347147-119347148	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181939578	chr11:119347203-119347204	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs72995127	chr11:119347295-119347296	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs368372305	chr11:119347307-119347308	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs529121199	chr11:119347308-119347309	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs144048259	chr11:119347343-119347344	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs542284746	chr11:119347346-119347347	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs57030511	chr11:119347363-119347364	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs186976978	chr11:119347373-119347374	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370148102	chr11:119347405-119347406	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373020191	chr11:119347422-119347423	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527994826	chr11:119347460-119347461	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs148681089	chr11:119347529-119347530	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs11605624	chr11:119347573-119347574	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs571042333	chr11:119347625-119347626	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs191768585	chr11:119347669-119347670	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs532083641	chr11:119347702-119347703	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs644613	chr11:119347715-119347716	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546498932	chr11:119347832-119347833	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370883843	chr11:119347862-119347863	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373995023	chr11:119347875-119347876	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550396764	chr11:119347894-119347895	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562400246	chr11:119347895-119347896	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs529806957	chr11:119347931-119347932	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs147660975	chr11:119347944-119347945	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547658035	chr11:119347955-119347956	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111820318	chr11:119347956-119347957	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183376852	chr11:119347961-119347962	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554144992	chr11:119347997-119347998	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187625928	chr11:119348028-119348029	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119337800-119359600	Weak transcription	Right Atrium	heart
2	chr11:119345200-119346600	Enhancers	HSMMtube	muscle
3	chr11:119345200-119346800	Enhancers	NHDF-Ad	bronchial
4	chr11:119345400-119346600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr11:119345400-119347600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:119345600-119346600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:119345600-119346600	Enhancers	K562	blood
8	chr11:119345600-119346600	Enhancers	Osteobl	bone
9	chr11:119345600-119346800	Enhancers	NHLF	lung
10	chr11:119346000-119346600	Enhancers	HSMM	muscle
11	chr11:119346000-119347600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr11:119346400-119346800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:119346400-119347200	Enhancers	Hela-S3	cervix
14	chr11:119346600-119350200	Weak transcription	K562	blood
15	chr11:119347600-119348000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr11:119347600-119348000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:119347600-119348400	Enhancers	HepG2	liver
18	chr11:119348000-119352200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:119348400-119350400	Weak transcription	HepG2	liver
20	chr11:119349400-119349800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr11:119349400-119349800	Enhancers	GM12878-XiMat	blood
22	chr11:119349800-119352000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr11:119350200-119352200	Enhancers	K562	blood
24	chr11:119350400-119351600	Enhancers	HepG2	liver
25	chr11:119350600-119350800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr11:119351000-119352600	Enhancers	Stomach Mucosa	stomach
27	chr11:119351200-119351400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:119351200-119352200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr11:119351200-119352600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:119351400-119351800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:119351400-119352000	Enhancers	HSMM	muscle
32	chr11:119351400-119352200	Enhancers	NHDF-Ad	bronchial
33	chr11:119351400-119352200	Enhancers	NHLF	lung
34	chr11:119351400-119352400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:119351400-119352400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr11:119351600-119351800	Enhancers	Fetal Muscle Leg	muscle
37	chr11:119351600-119352000	Bivalent Enhancer	Osteobl	bone
38	chr11:119351600-119352200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:119351600-119352200	Enhancers	A549	lung
40	chr11:119351600-119352200	Flanking Active TSS	HepG2	liver
41	chr11:119351600-119352600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:119351600-119352600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:119351600-119352600	Bivalent Enhancer	Adipose Nuclei	Adipose
44	chr11:119351600-119352600	Enhancers	NH-A	brain
45	chr11:119351600-119352800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:119351600-119355000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr11:119351800-119352000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:119351800-119352000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:119351800-119352000	Enhancers	Stomach Smooth Muscle	stomach
50	chr11:119351800-119352200	Enhancers	HUES6 Cell Line	embryonic stem cell

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