Variant report

Variant	nsv519914
Chromosome Location	chr11:86010789-86013361
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:479)
CpG islands
(count:488)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:86012970-86013907	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:86012946-86013380	K562	blood:	n/a	n/a
3	ATF1	chr11:86012997-86013477	K562	blood:	n/a	n/a
4	ATF2	chr11:86012805-86013806	GM12878	blood:	n/a	n/a
5	ATF2	chr11:86013018-86013591	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr11:86013058-86013434	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr11:86012954-86013424	GM12878	blood:	n/a	n/a
8	ATF3	chr11:86013014-86013744	A549	lung:	n/a	n/a
9	ATF3	chr11:86013085-86013343	HepG2	liver:	n/a	n/a
10	ATF3	chr11:86013073-86013503	K562	blood:	n/a	n/a
11	BCL3	chr11:86012880-86013874	A549	lung:	n/a	chr11:86013611-86013620
12	BCL3	chr11:86012843-86013670	A549	lung:	n/a	chr11:86013611-86013620
13	BCLAF1	chr11:86012942-86013616	GM12878	blood:	n/a	n/a
14	BCLAF1	chr11:86012949-86013577	K562	blood:	n/a	n/a
15	BCLAF1	chr11:86012947-86013619	K562	blood:	n/a	n/a
16	BCLAF1	chr11:86012955-86013709	GM12878	blood:	n/a	chr11:86013611-86013620
17	BHLHE40	chr11:86013020-86013704	K562	blood:	n/a	n/a
18	BRCA1	chr11:86012846-86013874	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr11:86012839-86013604	K562	blood:	n/a	n/a
20	CCNT2	chr11:86013076-86013499	K562	blood:	n/a	n/a
21	CEBPB	chr11:86013072-86013540	K562	blood:	n/a	n/a
22	CEBPB	chr11:86013105-86013456	K562	blood:	n/a	n/a
23	CEBPB	chr11:86013023-86013503	Hela-S3	cervix:	n/a	n/a
24	CHD1	chr11:86013007-86013728	GM12878	blood:	n/a	n/a
25	CHD2	chr11:86012950-86013831	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr11:86012960-86013877	GM12878	blood:	n/a	n/a
27	CHD2	chr11:86013049-86013728	K562	blood:	n/a	n/a
28	CHD2	chr11:86012989-86013669	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr11:86012995-86013568	HepG2	liver:	n/a	n/a
30	CREB1	chr11:86012929-86013704	HepG2	liver:	n/a	n/a
31	CREB1	chr11:86013022-86013399	A549	lung:	n/a	n/a
32	CREB1	chr11:86012944-86013539	A549	lung:	n/a	n/a
33	CTCF	chr11:86013260-86013410	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr11:86013100-86013250	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr11:86013240-86013510	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr11:86013260-86013410	AG10803	skin:	n/a	n/a
37	CTCF	chr11:86013360-86013630	Caco-2	colon:	n/a	n/a
38	CTCF	chr11:86013180-86013330	GM12871	blood:	n/a	n/a
39	CTCF	chr11:86013204-86013525	GM12878	blood:	n/a	n/a
40	CTCF	chr11:86013360-86013510	HepG2	liver:	n/a	n/a
41	CTCF	chr11:86013100-86013294	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr11:86013280-86013430	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr11:86013009-86013442	K562	blood:	n/a	n/a
44	CTCF	chr11:86013220-86013370	HMEC	breast:	n/a	n/a
45	CTCF	chr11:86013100-86013250	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr11:86013200-86013350	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr11:86013140-86013290	MCF-7	breast:	n/a	n/a
48	CUX1	chr11:86013027-86014241	K562	blood:	n/a	n/a
49	E2F4	chr11:86013033-86013577	K562	blood:	n/a	n/a
50	E2F4	chr11:86013017-86013444	MCF10A-Er-Src	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:86013179-86013229	SAEC	small airway:	n/a
2	chr11:86012876-86012926	Jurkat	blood:	n/a
3	chr11:86013232-86013282	LNCaP	prostate:	n/a
4	chr11:86013179-86013229	IMR90	lung:	fetal
5	chr11:86013179-86013229	MCF10A-Er-Src	breast:	n/a
6	chr11:86013224-86013274	U87	brain:	n/a
7	chr11:86013123-86013173	ECC-1	luminal epithelium:	n/a
8	chr11:86013348-86013398	HRE	kidney:	n/a
9	chr11:86013348-86013398	SKMC	muscle:	n/a
10	chr11:86013224-86013274	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:86012744-86012794	HRE	kidney:	n/a
12	chr11:86012876-86012926	GM12892	blood:	n/a
13	chr11:86013224-86013274	AG09309	skin:	n/a
14	chr11:86013232-86013282	NHBE	bronchial:	n/a
15	chr11:86013348-86013398	SK-N-MC	brain:	n/a
16	chr11:86013123-86013173	GM06990	blood:	n/a
17	chr11:86013232-86013282	HepG2	liver:	n/a
18	chr11:86013123-86013173	HEEpiC	esophagus:	n/a
19	chr11:86013123-86013173	SK-N-SH	brain:	n/a
20	chr11:86012744-86012794	BE2_C	brain:	n/a
21	chr11:86012876-86012926	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:86013348-86013398	AG04450	lung:	fetal
23	chr11:86013123-86013173	HRE	kidney:	n/a
24	chr11:86013348-86013398	AG09309	skin:	n/a
25	chr11:86013177-86013227	SK-N-SH	brain:	n/a
26	chr11:86013224-86013274	SK-N-MC	brain:	n/a
27	chr11:86013348-86013398	PANC-1	pancreas:	n/a
28	chr11:86012876-86012926	HMEC	breast:	n/a
29	chr11:86012876-86012926	HRCEpiC	kidney:	n/a
30	chr11:86013177-86013227	T-47D	breast:	n/a
31	chr11:86013179-86013229	HepG2	liver:	n/a
32	chr11:86012744-86012794	GM06990	blood:	n/a
33	chr11:86013232-86013282	ovcar-3	ovarian:	n/a
34	chr11:86013177-86013227	MCF-7	breast:	n/a
35	chr11:86013232-86013282	PFSK-1	brain:	n/a
36	chr11:86013177-86013227	HUVEC	blood vessel:	n/a
37	chr11:86013224-86013274	HEK293	kidney:	embryo
38	chr11:86013179-86013229	Hepatocyte	liver:	n/a
39	chr11:86013179-86013229	HCPEpiC	choroid plexus:	n/a
40	chr11:86013177-86013227	AG09309	skin:	n/a
41	chr11:86013177-86013227	GM12878	blood:	n/a
42	chr11:86013179-86013229	HCT-116	colon:	n/a
43	chr11:86012876-86012926	HAEpiC	amniotic membrane:	n/a
44	chr11:86012876-86012926	AG09319	gingival:	n/a
45	chr11:86013177-86013227	MCF10A-Er-Src	breast:	n/a
46	chr11:86013179-86013229	BE2_C	brain:	n/a
47	chr11:86013232-86013282	GM12891	blood:	n/a
48	chr11:86012744-86012794	H1-hESC	embryonic stem cell:	embryo
49	chr11:86013232-86013282	Hela-S3	cervix:	n/a
50	chr11:86013177-86013227	PFSK-1	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:85978505..85980119-chr11:86012077..86014955,2	K562	blood:
2	chr11:85954509..85956884-chr11:86013356..86015049,2	K562	blood:
3	chr11:86003733..86005993-chr11:86009757..86012694,4	K562	blood:
4	chr11:86010873..86013514-chr11:86034864..86037459,2	K562	blood:
5	chr11:85374267..85376584-chr11:86013241..86015955,2	MCF-7	breast:
6	chr11:85955907..85958640-chr11:86011728..86014261,2	MCF-7	breast:

No data

Variant related genes	Relation type
C11orf73	TF binding region
C11orf73	CpG island
ENSG00000255222	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000239856	chromatin interactions

Extended variants
information (count: 119 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:119 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7115858	chr11:86010789-86010790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574230423	chr11:86010838-86010839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7116227	chr11:86010856-86010857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs563546876	chr11:86010918-86010919	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577018152	chr11:86010932-86010933	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567319217	chr11:86010956-86010957	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs542552707	chr11:86010965-86010966	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76930582	chr11:86010974-86010975	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187320385	chr11:86010992-86010993	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs528471292	chr11:86010994-86010995	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs78064648	chr11:86011019-86011020	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370501425	chr11:86011035-86011036	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114783174	chr11:86011039-86011040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs531071001	chr11:86011071-86011072	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs146515717	chr11:86011097-86011098	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571032222	chr11:86011152-86011153	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs117353760	chr11:86011188-86011189	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs566274138	chr11:86011196-86011197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs190825538	chr11:86011206-86011207	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs530663335	chr11:86011210-86011211	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs141116776	chr11:86011216-86011217	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs3758881	chr11:86011256-86011257	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs74872595	chr11:86011273-86011274	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs291237	chr11:86011298-86011299	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs575206096	chr11:86011303-86011304	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187274225	chr11:86011307-86011308	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs146670388	chr11:86011318-86011319	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs545706576	chr11:86011329-86011330	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs559669986	chr11:86011373-86011374	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573214431	chr11:86011431-86011432	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs78865798	chr11:86011432-86011433	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs3758879	chr11:86011457-86011458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs533358276	chr11:86011475-86011476	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191682466	chr11:86011535-86011536	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs557662327	chr11:86011541-86011542	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533550808	chr11:86011546-86011547	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574136359	chr11:86011561-86011562	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182798072	chr11:86011618-86011619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs76669754	chr11:86011623-86011624	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs192502742	chr11:86011634-86011635	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184388495	chr11:86011639-86011640	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148842359	chr11:86011656-86011657	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs115924628	chr11:86011661-86011662	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143485331	chr11:86011680-86011681	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559883212	chr11:86011710-86011711	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs189607760	chr11:86011712-86011713	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573324728	chr11:86011715-86011716	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs291238	chr11:86011730-86011731	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs573128219	chr11:86011732-86011733	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs542154489	chr11:86011792-86011793	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	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
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	18438408	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85995600-86012600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:85995600-86012800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr11:85995800-86012600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:85995800-86013200	Weak transcription	Esophagus	oesophagus
5	chr11:85995800-86013200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr11:85996000-86012800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr11:85996000-86013000	Weak transcription	Fetal Intestine Large	intestine
8	chr11:86003000-86012600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:86003200-86013000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:86005400-86012600	Weak transcription	GM12878-XiMat	blood
11	chr11:86010400-86011200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:86011200-86011400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:86011400-86012400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:86012000-86012200	Enhancers	Dnd41	blood
15	chr11:86012000-86012600	Enhancers	Fetal Brain Female	brain
16	chr11:86012200-86012600	Enhancers	HepG2	liver
17	chr11:86012200-86012600	Enhancers	K562	blood
18	chr11:86012200-86013000	Flanking Active TSS	Dnd41	blood
19	chr11:86012200-86014800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:86012400-86012600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:86012400-86012600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:86012400-86012600	Enhancers	Brain Anterior Caudate	brain
23	chr11:86012400-86012600	Enhancers	Brain Cingulate Gyrus	brain
24	chr11:86012400-86012600	Enhancers	Brain Hippocampus Middle	brain
25	chr11:86012400-86012600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr11:86012400-86012600	Enhancers	A549	lung
27	chr11:86012400-86012600	Enhancers	Hela-S3	cervix
28	chr11:86012600-86012800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:86012600-86012800	Active TSS	Primary neutrophils fromperipheralblood	blood
30	chr11:86012600-86012800	Enhancers	Primary T cells from cord blood	blood
31	chr11:86012600-86012800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr11:86012600-86012800	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr11:86012600-86012800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:86012600-86012800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:86012600-86012800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr11:86012600-86012800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:86012600-86012800	Enhancers	Fetal Brain Male	brain
38	chr11:86012600-86012800	Enhancers	Fetal Lung	lung
39	chr11:86012600-86012800	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr11:86012600-86012800	Flanking Active TSS	A549	lung
41	chr11:86012600-86012800	Flanking Active TSS	GM12878-XiMat	blood
42	chr11:86012600-86012800	Enhancers	HUVEC	blood vessel
43	chr11:86012600-86012800	Flanking Active TSS	NH-A	brain
44	chr11:86012600-86012800	Flanking Active TSS	NHDF-Ad	bronchial
45	chr11:86012600-86012800	Enhancers	NHEK	skin
46	chr11:86012600-86013000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr11:86012600-86013000	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr11:86012600-86013000	Flanking Active TSS	Brain Cingulate Gyrus	brain
49	chr11:86012600-86013000	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr11:86012600-86013000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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