Variant report

Variant	rs10646198
Chromosome Location	chr11:76673261-76673262
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:76666896..76668570-chr11:76671083..76673989,2	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519700	chr11:76637651-76709407	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1042924	chr11:76659477-76709407	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1040833	chr11:76667160-76709407	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv396	chr11:76670116-76702745	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv3508597	chr11:76671304-76676202	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3508598	chr11:76671304-76676202	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv498761	chr11:76672826-76677823	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv14454	chr11:76672837-76674867	Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76631400-76688400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:76645800-76683800	Weak transcription	Esophagus	oesophagus
3	chr11:76646600-76688000	Weak transcription	HMEC	breast
4	chr11:76647200-76673800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:76647200-76674800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:76650600-76681200	Weak transcription	Brain Substantia Nigra	brain
7	chr11:76655800-76674200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:76655800-76681800	Weak transcription	Primary B cells from cord blood	blood
9	chr11:76656200-76677000	Weak transcription	Brain Anterior Caudate	brain
10	chr11:76657000-76674600	Weak transcription	Fetal Stomach	stomach
11	chr11:76657000-76676600	Weak transcription	Primary B cells from peripheral blood	blood
12	chr11:76657200-76688400	Weak transcription	Gastric	stomach
13	chr11:76659600-76673600	Weak transcription	Small Intestine	intestine
14	chr11:76659800-76673400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr11:76659800-76673600	Weak transcription	Primary T cells from cord blood	blood
16	chr11:76660000-76710800	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr11:76661200-76673800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:76661200-76674600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr11:76661800-76673400	Weak transcription	Pancreas	Pancrea
20	chr11:76662800-76673600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr11:76663000-76674600	Weak transcription	Liver	Liver
22	chr11:76665200-76673400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr11:76665800-76688400	Weak transcription	Right Ventricle	heart
24	chr11:76666800-76673600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:76666800-76677600	Weak transcription	Hela-S3	cervix
26	chr11:76666800-76695400	Weak transcription	NHEK	skin
27	chr11:76667400-76673800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr11:76667600-76673400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr11:76667800-76673800	Weak transcription	Brain Angular Gyrus	brain
30	chr11:76667800-76674400	Weak transcription	Fetal Muscle Leg	muscle
31	chr11:76668400-76673400	Weak transcription	Dnd41	blood
32	chr11:76668600-76673400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:76668600-76673600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr11:76668800-76673600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr11:76668800-76674000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr11:76669000-76675200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr11:76669600-76673800	Weak transcription	Colonic Mucosa	Colon
38	chr11:76669600-76674200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:76670000-76673800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr11:76670000-76674400	Weak transcription	A549	lung
41	chr11:76670200-76673600	Weak transcription	GM12878-XiMat	blood
42	chr11:76670200-76675200	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr11:76670400-76673400	Weak transcription	Stomach Mucosa	stomach
44	chr11:76670400-76673800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr11:76670600-76674000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr11:76671200-76673600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr11:76671200-76673600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:76671600-76673800	Weak transcription	K562	blood
49	chr11:76671600-76675400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr11:76672000-76674800	Weak transcription	Colon Smooth Muscle	Colon

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