Variant report

Variant	rs7806963
Chromosome Location	chr7:138195280-138195281
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:138194615-138195529	HepG2	liver:	n/a	n/a
2	POLR2A	chr7:138195092-138195319	ProgFib	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:138194787..138197500-chr7:138199534..138201806,2	MCF-7	breast:
2	chr7:138190873..138192448-chr7:138192616..138195526,2	K562	blood:
3	chr7:138194009..138196443-chr7:138197164..138199036,2	MCF-7	breast:

Variant related genes	Relation type
TRIM24	TF binding region

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10239358	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10488642	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35668636	0.81[EUR][1000 genomes]
rs68115887	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7799136	0.84[EUR][1000 genomes]
rs7810516	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831153	chr7:138078179-138265648	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv1030956	chr7:138163169-138579519	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138161800-138195800	Weak transcription	Fetal Brain Female	brain
2	chr7:138164000-138199800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:138168000-138196200	Weak transcription	Left Ventricle	heart
4	chr7:138175200-138201200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr7:138176600-138203600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr7:138177000-138212600	Weak transcription	Pancreas	Pancrea
7	chr7:138178600-138212200	Weak transcription	NHLF	lung
8	chr7:138180200-138204200	Weak transcription	Brain Substantia Nigra	brain
9	chr7:138182200-138196200	Weak transcription	Spleen	Spleen
10	chr7:138183000-138196400	Weak transcription	Fetal Lung	lung
11	chr7:138183000-138203600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:138184400-138196200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:138184400-138196200	Weak transcription	Fetal Muscle Trunk	muscle
14	chr7:138184400-138196400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:138184400-138196400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr7:138184400-138197000	Weak transcription	Aorta	Aorta
17	chr7:138184400-138198600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr7:138184600-138196800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:138184800-138196200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:138184800-138204000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr7:138185000-138198600	Weak transcription	Fetal Heart	heart
22	chr7:138186000-138196200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:138186600-138210400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr7:138187200-138196400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr7:138187200-138196400	Weak transcription	Brain Hippocampus Middle	brain
26	chr7:138187400-138196200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr7:138187400-138197000	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr7:138187400-138203800	Weak transcription	Psoas Muscle	Psoas
29	chr7:138187600-138197200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr7:138187600-138202600	Weak transcription	Hela-S3	cervix
31	chr7:138187600-138203600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:138187800-138196400	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr7:138188000-138196200	Weak transcription	Adipose Nuclei	Adipose
34	chr7:138188000-138197200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:138188000-138204200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr7:138188200-138203800	Weak transcription	Colonic Mucosa	Colon
37	chr7:138188400-138196800	Strong transcription	K562	blood
38	chr7:138188400-138201800	Weak transcription	NH-A	brain
39	chr7:138188400-138209800	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr7:138188600-138195400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:138188600-138196200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr7:138188600-138196400	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr7:138188600-138196400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr7:138188600-138203600	Weak transcription	Stomach Smooth Muscle	stomach
45	chr7:138188800-138195800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:138188800-138196400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr7:138188800-138210400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr7:138188800-138210600	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr7:138189000-138195400	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr7:138189000-138195800	Strong transcription	Fetal Thymus	thymus

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