Variant report

Variant	rs7764120
Chromosome Location	chr6:34310190-34310191
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34308267..34311502-chr6:34313780..34316538,3	K562	blood:
2	chr6:34309301..34312552-chr6:34312659..34315940,4	K562	blood:
3	chr6:34214571..34216737-chr6:34309233..34311711,2	K562	blood:
4	chr6:34238995..34241541-chr6:34307534..34310949,3	K562	blood:
5	chr6:34303920..34306349-chr6:34307899..34311010,3	K562	blood:
6	chr6:34305250..34307284-chr6:34307723..34310637,2	MCF-7	breast:
7	chr6:34307128..34308911-chr6:34309143..34310713,2	K562	blood:

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs57642915	0.84[AFR][1000 genomes]
rs58678278	0.84[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1798756	chr6:34203406-34319041	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	esv1798835	chr6:34204183-34319041	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv1792088	chr6:34204285-34318837	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv1793127	chr6:34204285-34319041	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34261800-34330800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr6:34284800-34310800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr6:34285200-34330600	Weak transcription	Thymus	Thymus
4	chr6:34285800-34326600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr6:34289000-34325200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:34297400-34312800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr6:34298600-34326400	Weak transcription	A549	lung
8	chr6:34299400-34310800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:34301600-34318000	Weak transcription	Fetal Brain Female	brain
10	chr6:34303000-34312800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:34304600-34310400	Enhancers	Colon Smooth Muscle	Colon
12	chr6:34304600-34310600	Enhancers	Rectal Smooth Muscle	rectum
13	chr6:34304800-34310200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr6:34305000-34310600	Enhancers	Fetal Heart	heart
15	chr6:34305400-34311200	Enhancers	Psoas Muscle	Psoas
16	chr6:34306000-34310400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:34306000-34313800	Weak transcription	NHEK	skin
18	chr6:34306000-34327800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:34306000-34328800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr6:34306200-34311000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr6:34306400-34310800	Strong transcription	Primary T cells from cord blood	blood
22	chr6:34306400-34310800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr6:34306600-34310600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:34306600-34312200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:34307000-34311000	Weak transcription	Spleen	Spleen
26	chr6:34307000-34312400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:34307000-34320000	Weak transcription	Ovary	ovary
28	chr6:34307400-34314200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr6:34307600-34310800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr6:34308000-34310400	Enhancers	Stomach Mucosa	stomach
31	chr6:34308000-34310800	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr6:34308200-34310200	Strong transcription	Primary hematopoietic stem cells	blood
33	chr6:34308200-34310600	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr6:34308400-34310200	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr6:34308400-34310800	Enhancers	Brain Substantia Nigra	brain
36	chr6:34308400-34312400	Enhancers	HUVEC	blood vessel
37	chr6:34308600-34310200	Enhancers	NHLF	lung
38	chr6:34308600-34310400	Enhancers	Right Ventricle	heart
39	chr6:34308600-34310800	Enhancers	Brain Anterior Caudate	brain
40	chr6:34308800-34310200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr6:34308800-34310600	Enhancers	Fetal Kidney	kidney
42	chr6:34308800-34313600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr6:34308800-34330800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:34309000-34310200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:34309000-34311800	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr6:34309200-34310600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:34309200-34315800	Weak transcription	Placenta	Placenta
48	chr6:34309200-34318200	Weak transcription	Fetal Lung	lung
49	chr6:34309400-34310200	Enhancers	Fetal Brain Male	brain
50	chr6:34309400-34310400	Enhancers	Brain Angular Gyrus	brain

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