Variant report

Variant	nsv975200
Chromosome Location	chr11:71277624-71280675
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:71278836-71278905	GM12892	blood:	n/a	n/a
2	CTCF	chr11:71278725-71278863	HepG2	liver:	n/a	chr11:71278817-71278838
3	CTCF	chr11:71278704-71278873	K562	blood:	n/a	chr11:71278817-71278838
4	CTCF	chr11:71279653-71279762	MCF-7	breast:	n/a	n/a
5	CTCF	chr11:71278840-71278990	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr11:71278802-71278890	MCF-7	breast:	n/a	chr11:71278817-71278838
7	CTCF	chr11:71278840-71278990	HMF	breast:	n/a	n/a
8	CTCF	chr11:71278820-71278970	MCF-7	breast:	n/a	n/a
9	CTCF	chr11:71278800-71278950	HCPEpiC	choroid plexus:	n/a	chr11:71278817-71278838
10	CTCF	chr11:71278860-71279010	NB4	blood:	n/a	n/a
11	CTCF	chr11:71278880-71279030	NHDF-neo	bronchial:	n/a	n/a
12	CTCF	chr11:71278860-71279010	HAc	cerebellar:	n/a	n/a
13	CTCF	chr11:71279640-71279790	MCF-7	breast:	n/a	n/a
14	CTCF	chr11:71278795-71278913	HepG2	liver:	n/a	chr11:71278817-71278838
15	CTCF	chr11:71278820-71278970	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr11:71278860-71279010	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr11:71279657-71279768	MCF-7	breast:	n/a	n/a
18	CTCF	chr11:71279355-71279463	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr11:71279620-71279770	NHEK	skin:	n/a	n/a
20	CTCF	chr11:71280593-71280657	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr11:71278704-71278947	A549	lung:	n/a	chr11:71278817-71278838
22	CTCF	chr11:71278840-71278990	HEK293	kidney:	n/a	n/a
23	CTCF	chr11:71278800-71278950	HPAF	blood vessel:	n/a	chr11:71278817-71278838
24	CTCF	chr11:71279660-71279810	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:71278606-71279019	K562	blood:	n/a	chr11:71278817-71278838
26	CTCF	chr11:71279520-71279670	NHEK	skin:	n/a	n/a
27	CTCF	chr11:71278840-71278990	HRE	kidney:	n/a	n/a
28	CTCF	chr11:71278104-71278131	GM10248	blood:	n/a	n/a
29	CTCF	chr11:71278802-71278843	GM12878	blood:	n/a	chr11:71278817-71278838
30	CTCF	chr11:71278860-71279010	HepG2	liver:	n/a	n/a
31	CTCF	chr11:71279661-71279749	MCF-7	breast:	n/a	n/a
32	CTCF	chr11:71279680-71279740	MCF-7	breast:	n/a	n/a
33	CTCF	chr11:71278840-71278990	GM12864	blood:	n/a	n/a
34	CTCF	chr11:71278860-71279010	BJ	skin:	n/a	n/a
35	CTCF	chr11:71278353-71278395	GM10248	blood:	n/a	n/a
36	CTCF	chr11:71278768-71278811	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr11:71278860-71279010	A549	lung:	n/a	n/a
38	CTCF	chr11:71278695-71278895	GM12878	blood:	n/a	chr11:71278817-71278838
39	CTCF	chr11:71278800-71278950	HCM	heart:	n/a	chr11:71278817-71278838
40	CTCF	chr11:71278564-71278652	LNCaP	prostate:	n/a	n/a
41	CTCF	chr11:71278424-71278483	LNCaP	prostate:	n/a	n/a
42	CTCF	chr11:71278780-71278930	HRE	kidney:	n/a	chr11:71278817-71278838
43	CTCF	chr11:71278760-71278910	WERI-Rb-1	eye:	n/a	chr11:71278817-71278838
44	CTCF	chr11:71278800-71278950	HEEpiC	esophagus:	n/a	chr11:71278817-71278838
45	CTCF	chr11:71278761-71278875	Hela-S3	cervix:	n/a	chr11:71278817-71278838
46	CTCF	chr11:71279659-71279765	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:71278760-71278896	MCF-7	breast:	n/a	chr11:71278817-71278838
48	CTCF	chr11:71278840-71278990	HBMEC	blood vessel:	n/a	n/a
49	EBF1	chr11:71279064-71279083	GM12878	blood:	n/a	n/a
50	EP300	chr11:71279462-71279902	MCF-7	breast:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71278406..71279386-chr11:71291430..71292089,2	MCF-7	breast:
2	chr11:71278628..71280477-chr11:71289049..71291000,2	MCF-7	breast:
3	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
4	chr11:71279845..71280406-chr11:71290008..71290749,2	MCF-7	breast:
5	chr11:71159116..71165503-chr11:71274687..71279227,9	MCF-7	breast:
6	chr11:71279425..71280036-chr11:71290519..71291383,2	MCF-7	breast:
7	chr11:71158604..71160379-chr11:71280505..71283180,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTAP5-10-1	chr11:71279726-71279980	NONHSAT022692

No data

Variant related genes	Relation type
ENSG00000248903	TF binding region
ENSG00000249387	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000172893	chromatin interactions
ENSG00000254682	chromatin interactions

Extended variants
information (count: 189 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:189 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550457064	chr11:71277628-71277629	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs71946973	chr11:71277648-71277649	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs201171826	chr11:71277651-71277652	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs75544717	chr11:71277652-71277653	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs539220182	chr11:71277665-71277666	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs530931284	chr11:71277744-71277745	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs117393523	chr11:71277777-71277778	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs536949726	chr11:71277821-71277822	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs369284443	chr11:71277841-71277842	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs374056111	chr11:71277871-71277872	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs184908574	chr11:71277902-71277903	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs150461342	chr11:71277905-71277906	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs377361112	chr11:71277917-71277918	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs34678580	chr11:71277946-71277947	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs66743503	chr11:71277947-71277948	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs71272259	chr11:71277948-71277949	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs559468601	chr11:71277958-71277959	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs188225724	chr11:71277959-71277960	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs550905026	chr11:71277963-71277964	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs547659658	chr11:71277968-71277969	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs546382540	chr11:71277972-71277973	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs564532435	chr11:71277980-71277981	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs11234218	chr11:71277981-71277982	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs373917868	chr11:71277983-71277984	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs73530497	chr11:71278015-71278016	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs138189121	chr11:71278016-71278017	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs373812282	chr11:71278023-71278024	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs367943244	chr11:71278026-71278027	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs370501530	chr11:71278030-71278031	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs7930916	chr11:71278046-71278047	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs547411821	chr11:71278054-71278055	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs192173505	chr11:71278112-71278113	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs566026332	chr11:71278113-71278114	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs539555600	chr11:71278132-71278133	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs7930212	chr11:71278139-71278140	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs7930224	chr11:71278162-71278163	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs537291358	chr11:71278166-71278167	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs555357601	chr11:71278167-71278168	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs573907487	chr11:71278168-71278169	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs534571060	chr11:71278220-71278221	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs556470273	chr11:71278223-71278224	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs577769622	chr11:71278238-71278239	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs184613416	chr11:71278279-71278280	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs58875192	chr11:71278287-71278288	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs189451814	chr11:71278294-71278295	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs544023548	chr11:71278366-71278367	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs562218725	chr11:71278367-71278368	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs529561018	chr11:71278368-71278369	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs540987366	chr11:71278377-71278378	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs559326362	chr11:71278412-71278413	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71276600-71278200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr11:71277000-71279200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr11:71277200-71277800	Enhancers	Fetal Brain Male	brain
4	chr11:71277200-71278000	Bivalent Enhancer	Fetal Stomach	stomach
5	chr11:71277200-71278200	Enhancers	Spleen	Spleen
6	chr11:71277200-71280400	Enhancers	Adipose Nuclei	Adipose
7	chr11:71277400-71277800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
8	chr11:71277400-71278000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:71277400-71278000	Enhancers	Lung	lung
10	chr11:71277400-71278400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr11:71277400-71279800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:71277600-71278000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr11:71277600-71278000	Bivalent Enhancer	HepG2	liver
14	chr11:71277600-71278200	Enhancers	H9 Cell Line	embryonic stem cell
15	chr11:71277600-71279000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr11:71277600-71279000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:71277600-71279800	Weak transcription	Left Ventricle	heart
18	chr11:71277600-71280400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:71277600-71281600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:71277600-71282800	Weak transcription	Fetal Intestine Small	intestine
21	chr11:71277600-71290400	Weak transcription	Right Atrium	heart
22	chr11:71277800-71278000	Enhancers	Fetal Brain Female	brain
23	chr11:71277800-71278800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr11:71278000-71278800	Enhancers	HepG2	liver
25	chr11:71278000-71279800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr11:71278200-71278800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr11:71278200-71281600	Weak transcription	Spleen	Spleen
28	chr11:71278400-71279800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr11:71278800-71279000	Bivalent Enhancer	Fetal Stomach	stomach
30	chr11:71278800-71279000	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr11:71278800-71279200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:71278800-71279400	Enhancers	H9 Cell Line	embryonic stem cell
33	chr11:71278800-71279600	Bivalent Enhancer	HepG2	liver
34	chr11:71279000-71279400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr11:71279000-71280200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:71279000-71280600	Enhancers	Fetal Muscle Leg	muscle
37	chr11:71279000-71281200	Enhancers	Fetal Stomach	stomach
38	chr11:71279200-71279600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr11:71279200-71280400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:71279400-71280000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr11:71279400-71281400	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr11:71279600-71280200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr11:71279600-71280200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr11:71279600-71280200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:71279600-71280200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:71279600-71280200	Enhancers	Psoas Muscle	Psoas
47	chr11:71279600-71280200	Enhancers	Stomach Smooth Muscle	stomach
48	chr11:71279600-71280200	Flanking Bivalent TSS/Enh	HepG2	liver
49	chr11:71279600-71280400	Enhancers	Fetal Lung	lung
50	chr11:71279600-71282000	Enhancers	Skeletal Muscle Female	skeletal muscle

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