Variant report

Variant	rs138701565
Chromosome Location	chr5:74670726-74670727
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	TCF7L2	chr5:74669804-74670898	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:74631027..74633689-chr5:74669899..74673257,3	MCF-7	breast:

Variant related genes	Relation type
COL4A3BP	TF binding region
ENSG00000113161	Chromatin interaction
ENSG00000247372	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv882192	chr5:74641707-74707762	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv882193	chr5:74656175-74917862	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv882194	chr5:74656175-74946455	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv980685	chr5:74669881-74670738	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74656400-74673600	Weak transcription	Psoas Muscle	Psoas
2	chr5:74656400-74673600	Weak transcription	Small Intestine	intestine
3	chr5:74656400-74673600	Weak transcription	Spleen	Spleen
4	chr5:74656400-74674000	Weak transcription	Brain Germinal Matrix	brain
5	chr5:74656400-74674800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr5:74656400-74674800	Weak transcription	Brain Substantia Nigra	brain
7	chr5:74656400-74676800	Weak transcription	Fetal Brain Male	brain
8	chr5:74656400-74687200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:74656400-74725600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr5:74656600-74675600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr5:74656600-74675800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:74656600-74675800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr5:74656600-74676800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr5:74656600-74677200	Weak transcription	Aorta	Aorta
15	chr5:74656600-74694800	Weak transcription	Brain Angular Gyrus	brain
16	chr5:74656800-74676200	Weak transcription	Colonic Mucosa	Colon
17	chr5:74656800-74731400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr5:74657400-74674800	Weak transcription	A549	lung
19	chr5:74657600-74673600	Weak transcription	Lung	lung
20	chr5:74657800-74708000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr5:74658000-74674800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr5:74658400-74673200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr5:74658600-74673200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr5:74658600-74674800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr5:74658600-74674800	Weak transcription	Fetal Kidney	kidney
26	chr5:74659000-74674600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr5:74659200-74674800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr5:74659600-74673600	Weak transcription	Esophagus	oesophagus
29	chr5:74659600-74673600	Weak transcription	Gastric	stomach
30	chr5:74659600-74675800	Weak transcription	Brain Hippocampus Middle	brain
31	chr5:74659800-74673600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:74659800-74677000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:74659800-74684800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr5:74659800-74720600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr5:74660000-74674600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr5:74660000-74722800	Weak transcription	Fetal Heart	heart
37	chr5:74660200-74673600	Weak transcription	Fetal Muscle Leg	muscle
38	chr5:74660200-74707800	Weak transcription	Stomach Mucosa	stomach
39	chr5:74660400-74673600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:74661800-74683600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr5:74663200-74676800	Weak transcription	K562	blood
42	chr5:74664600-74674400	Weak transcription	NH-A	brain
43	chr5:74664600-74674600	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr5:74664600-74676800	Weak transcription	NHLF	lung
45	chr5:74664600-74677000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:74664800-74670800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:74664800-74677000	Weak transcription	HUVEC	blood vessel
48	chr5:74665000-74703000	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr5:74667000-74723200	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr5:74667200-74670800	Strong transcription	Primary hematopoietic stem cells	blood

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