Variant report

Variant	nsv526053
Chromosome Location	chr11:74857436-74861545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr11:74858583-74858836	K562	blood:	n/a	n/a
2	CEBPB	chr11:74857822-74858095	HepG2	liver:	n/a	chr11:74858004-74858015
3	CEBPB	chr11:74857925-74858160	Hela-S3	cervix:	n/a	chr11:74858004-74858015
4	CEBPB	chr11:74857855-74858155	IMR90	lung:	n/a	chr11:74858004-74858015
5	CEBPB	chr11:74857899-74858098	HepG2	liver:	n/a	chr11:74858004-74858015
6	CEBPB	chr11:74857960-74858121	H1-hESC	embryonic stem cell:	n/a	chr11:74858004-74858015
7	CEBPB	chr11:74857850-74858185	HepG2	liver:	n/a	chr11:74858004-74858015
8	CEBPB	chr11:74857916-74858186	K562	blood:	n/a	chr11:74858004-74858015
9	CTCF	chr11:74859100-74859250	GM12866	blood:	n/a	n/a
10	EGR1	chr11:74859085-74859362	K562	blood:	n/a	chr11:74859210-74859223
11	EP300	chr11:74858589-74858828	K562	blood:	n/a	n/a
12	EP300	chr11:74858156-74859222	SK-N-SH	brain:	n/a	chr11:74858397-74858410
13	EP300	chr11:74858555-74858842	SK-N-SH_RA	brain:	n/a	n/a
14	GABPA	chr11:74858931-74859366	HL-60	blood:	n/a	chr11:74859209-74859218 chr11:74859030-74859039
15	GATA1	chr11:74858351-74859055	K562	blood:	n/a	n/a
16	GATA2	chr11:74858060-74858983	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr11:74858541-74858765	SH-SY5Y	brain:	n/a	n/a
18	HEY1	chr11:74856893-74857449	K562	blood:	n/a	n/a
19	JUND	chr11:74857920-74858122	HepG2	liver:	n/a	n/a
20	JUND	chr11:74858587-74858923	K562	blood:	n/a	n/a
21	MAFF	chr11:74858992-74859170	HepG2	liver:	n/a	chr11:74859139-74859157
22	MAFK	chr11:74859071-74859247	HepG2	liver:	n/a	chr11:74859124-74859139 chr11:74859141-74859152 chr11:74859141-74859156
23	MAFK	chr11:74859052-74859188	HepG2	liver:	n/a	chr11:74859124-74859139 chr11:74859141-74859152 chr11:74859141-74859156
24	MAZ	chr11:74858694-74858702	K562	blood:	n/a	n/a
25	MYC	chr11:74858632-74858809	K562	blood:	n/a	n/a
26	MYC	chr11:74858986-74859038	MCF-7	breast:	n/a	n/a
27	POLR2A	chr11:74857839-74857953	K562	blood:	n/a	n/a
28	POLR2A	chr11:74859009-74859066	ProgFib	skin:	n/a	n/a
29	POLR2A	chr11:74858501-74858557	MCF-7	breast:	n/a	n/a
30	POLR2A	chr11:74860804-74860985	K562	blood:	n/a	n/a
31	RCOR1	chr11:74858563-74858852	K562	blood:	n/a	n/a
32	SPI1	chr11:74859038-74859386	HL-60	blood:	n/a	chr11:74859194-74859207
33	SPI1	chr11:74859020-74859234	K562	blood:	n/a	chr11:74859194-74859207
34	SPI1	chr11:74858930-74859361	HL-60	blood:	n/a	chr11:74859194-74859207
35	TAF7	chr11:74857194-74857483	K562	blood:	n/a	n/a
36	TAL1	chr11:74858649-74858844	K562	blood:	n/a	n/a
37	TBL1XR1	chr11:74858670-74858758	K562	blood:	n/a	n/a
38	TBP	chr11:74857278-74857500	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:74861433-74861483	SKMC	muscle:	n/a
2	chr11:74860623-74860673	HRCEpiC	kidney:	n/a
3	chr11:74860985-74861035	GM06990	blood:	n/a
4	chr11:74861433-74861483	GM19239	blood:	n/a
5	chr11:74860985-74861035	GM12892	blood:	n/a
6	chr11:74861433-74861483	NB4	blood:	n/a
7	chr11:74860623-74860673	K562	blood:	n/a
8	chr11:74861433-74861483	AG09319	gingival:	n/a
9	chr11:74860985-74861035	U87	brain:	n/a
10	chr11:74860985-74861035	NT2-D1	testis:	n/a
11	chr11:74861433-74861483	MCF10A-Er-Src	breast:	n/a
12	chr11:74860623-74860673	LNCaP	prostate:	n/a
13	chr11:74860623-74860673	U87	brain:	n/a
14	chr11:74860623-74860673	HIPEpiC	eye:	n/a
15	chr11:74861433-74861483	NT2-D1	testis:	n/a
16	chr11:74860985-74861035	AG09319	gingival:	n/a
17	chr11:74860623-74860673	HCT-116	colon:	n/a
18	chr11:74860623-74860673	CMK	blood:	n/a
19	chr11:74860985-74861035	IMR90	lung:	fetal
20	chr11:74861433-74861483	NH-A	brain:	n/a
21	chr11:74861433-74861483	T-47D	breast:	n/a
22	chr11:74861433-74861483	ovcar-3	ovarian:	n/a
23	chr11:74861433-74861483	Hela-S3	cervix:	n/a
24	chr11:74860623-74860673	Hela-S3	cervix:	n/a
25	chr11:74861433-74861483	HCM	heart:	n/a
26	chr11:74861433-74861483	MCF-7	breast:	n/a
27	chr11:74861433-74861483	HRPEpiC	eye:	n/a
28	chr11:74860623-74860673	HRE	kidney:	n/a
29	chr11:74861433-74861483	HNPCEpiC	eye:	n/a
30	chr11:74861433-74861483	AG10803	skin:	n/a
31	chr11:74860623-74860673	BE2_C	brain:	n/a
32	chr11:74860985-74861035	HUVEC	blood vessel:	n/a
33	chr11:74860623-74860673	PANC-1	pancreas:	n/a
34	chr11:74860623-74860673	H1-hESC	embryonic stem cell:	embryo
35	chr11:74860985-74861035	Hela-S3	cervix:	n/a
36	chr11:74861433-74861483	HMEC	breast:	n/a
37	chr11:74861433-74861483	HAEpiC	amniotic membrane:	n/a
38	chr11:74861433-74861483	NHDF-neo	bronchial:	n/a
39	chr11:74861433-74861483	HCPEpiC	choroid plexus:	n/a
40	chr11:74860985-74861035	AG09309	skin:	n/a
41	chr11:74860623-74860673	NT2-D1	testis:	n/a
42	chr11:74860985-74861035	ProgFib	skin:	n/a
43	chr11:74860985-74861035	HNPCEpiC	eye:	n/a
44	chr11:74860985-74861035	HCF	heart:	n/a
45	chr11:74860985-74861035	SK-N-SH_RA	brain:	n/a
46	chr11:74860623-74860673	NB4	blood:	n/a
47	chr11:74861433-74861483	HEK293	kidney:	embryo
48	chr11:74861433-74861483	GM06990	blood:	n/a
49	chr11:74860623-74860673	SK-N-SH	brain:	n/a
50	chr11:74861433-74861483	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:74860426..74862138-chr11:74866873..74869626,2	K562	blood:
2	chr11:74856790..74858510-chr11:74872953..74874736,2	K562	blood:
3	chr11:74851665..74854336-chr11:74855499..74858438,2	MCF-7	breast:
4	chr11:74855263..74857474-chr11:74861405..74863730,2	MCF-7	breast:
5	chr11:74856690..74858303-chr11:74861317..74863016,2	K562	blood:
6	chr11:74860499..74862617-chr11:74862814..74864502,2	K562	blood:
7	chr11:74853654..74855652-chr11:74858777..74860606,2	K562	blood:
8	chr11:74860782..74862620-chr11:74866728..74869676,2	MCF-7	breast:
9	chr11:74855408..74858303-chr11:74861375..74864283,3	K562	blood:
10	chr11:74850392..74852587-chr11:74855694..74858278,2	MCF-7	breast:
11	chr11:74856309..74859040-chr11:74914787..74916343,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLCO2B1	TF binding region
SLCO2B1	CpG island
ENSG00000255395	chromatin interactions
ENSG00000137491	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:170 , 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	rs10899076	chr11:74857436-74857437	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138833762	chr11:74857443-74857444	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575175187	chr11:74857445-74857446	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs34965748	chr11:74857450-74857451	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs188578219	chr11:74857458-74857459	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs371774079	chr11:74857478-74857479	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs76524695	chr11:74857479-74857480	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs574419336	chr11:74857485-74857486	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs540345420	chr11:74857502-74857503	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541347661	chr11:74857526-74857527	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560625802	chr11:74857563-74857564	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532754051	chr11:74857571-74857572	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs142024867	chr11:74857586-74857587	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs367908464	chr11:74857590-74857591	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576343760	chr11:74857597-74857598	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563076632	chr11:74857600-74857601	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531718783	chr11:74857621-74857622	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs543681153	chr11:74857636-74857637	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191729742	chr11:74857671-74857672	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs66903340	chr11:74857732-74857733	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs182650234	chr11:74857747-74857748	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs386755056	chr11:74857788-74857789	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2187435	chr11:74857789-74857790	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs78632064	chr11:74857861-74857862	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs574876115	chr11:74857876-74857877	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs11236354	chr11:74857880-74857881	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs558421107	chr11:74857914-74857915	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs146340867	chr11:74857915-74857916	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs11822379	chr11:74857916-74857917	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs187339662	chr11:74857928-74857929	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs115933135	chr11:74857938-74857939	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs559568882	chr11:74857968-74857969	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138393654	chr11:74858026-74858027	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs553952751	chr11:74858070-74858071	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs528270150	chr11:74858098-74858099	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577502110	chr11:74858125-74858126	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs546456222	chr11:74858131-74858132	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs563177460	chr11:74858136-74858137	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs531510870	chr11:74858173-74858174	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs191262984	chr11:74858212-74858213	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs4944990	chr11:74858213-74858214	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs116149094	chr11:74858264-74858265	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs2712805	chr11:74858285-74858286	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs149618792	chr11:74858344-74858345	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs183849954	chr11:74858345-74858346	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs532152488	chr11:74858352-74858353	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs188659866	chr11:74858358-74858359	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs569049822	chr11:74858383-74858384	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537708394	chr11:74858404-74858405	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548465526	chr11:74858431-74858432	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	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
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
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74852000-74861600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:74852400-74858200	Weak transcription	Esophagus	oesophagus
3	chr11:74852400-74861000	Weak transcription	Stomach Mucosa	stomach
4	chr11:74853800-74857800	Enhancers	Duodenum Mucosa	Duodenum
5	chr11:74853800-74860200	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr11:74853800-74862000	Enhancers	HepG2	liver
7	chr11:74853800-74862200	Enhancers	Placenta	Placenta
8	chr11:74854000-74862000	Enhancers	Fetal Intestine Large	intestine
9	chr11:74854400-74857600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:74854400-74858400	Weak transcription	Left Ventricle	heart
11	chr11:74854400-74858400	Weak transcription	Right Atrium	heart
12	chr11:74854400-74858400	Weak transcription	Right Ventricle	heart
13	chr11:74855200-74862200	Enhancers	Fetal Intestine Small	intestine
14	chr11:74855400-74857800	Weak transcription	Brain Anterior Caudate	brain
15	chr11:74855600-74858200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr11:74855600-74858200	Weak transcription	Spleen	Spleen
17	chr11:74855600-74861200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr11:74855600-74861600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr11:74855800-74857800	Weak transcription	Fetal Muscle Leg	muscle
20	chr11:74855800-74858000	Weak transcription	Fetal Thymus	thymus
21	chr11:74855800-74858200	Weak transcription	Liver	Liver
22	chr11:74855800-74858200	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr11:74855800-74858400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:74855800-74858800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:74855800-74858800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:74856000-74857800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr11:74856000-74857800	Weak transcription	Lung	lung
28	chr11:74856000-74858400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:74856000-74858800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:74856200-74860200	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr11:74856400-74859200	Enhancers	K562	blood
32	chr11:74856400-74859600	Enhancers	Colonic Mucosa	Colon
33	chr11:74856600-74858600	Weak transcription	Brain Hippocampus Middle	brain
34	chr11:74856600-74863400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr11:74857000-74857800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr11:74857000-74859400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:74857000-74860000	Enhancers	Adipose Nuclei	Adipose
38	chr11:74857400-74858600	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr11:74857400-74859000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:74857400-74865600	Weak transcription	Small Intestine	intestine
41	chr11:74857600-74859200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:74857800-74858000	Enhancers	Fetal Brain Male	brain
43	chr11:74857800-74858200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr11:74857800-74859000	Enhancers	Brain Anterior Caudate	brain
45	chr11:74857800-74859000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr11:74857800-74859800	Enhancers	Lung	lung
47	chr11:74857800-74860000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr11:74857800-74860000	Enhancers	Fetal Muscle Leg	muscle
49	chr11:74858000-74860000	Enhancers	Fetal Thymus	thymus
50	chr11:74858200-74858400	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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