Variant report

Variant	rs374134322
Chromosome Location	chr7:127992631-127992632
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:127913044..127915335-chr7:127992240..127993797,2	K562	blood:
2	chr7:127982362..127984093-chr7:127992558..127995177,2	MCF-7	breast:
3	chr7:127992082..127994842-chr7:128029852..128032073,3	K562	blood:
4	chr7:127991141..127992839-chr7:127994705..127996789,2	K562	blood:
5	chr7:127991366..127994024-chr7:128043905..128046118,2	MCF-7	breast:
6	chr7:127990878..127995208-chr7:127998293..128004686,6	K562	blood:
7	chr7:127992585..127993570-chr7:128027268..128027996,2	K562	blood:
8	chr7:127992322..127995114-chr7:128014039..128015819,2	K562	blood:
9	chr7:127986655..127989567-chr7:127989980..127992814,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000224940	Chromatin interaction
ENSG00000106348	Chromatin interaction
ENSG00000106344	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831124	chr7:127970345-128147910	Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	nsv889191	chr7:127973133-128073326	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv608400	chr7:127978820-128048194	Weak transcription Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
4	esv2493565	chr7:127985695-128053377	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	esv3478325	chr7:127986726-128053483	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	esv3478326	chr7:127986726-128053483	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	esv3355435	chr7:127989716-127994314	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	esv3406494	chr7:127990366-127992864	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	esv3386261	chr7:127991266-127993364	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127990400-127994400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:127991000-127992800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:127991000-127993000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr7:127991200-127992800	Enhancers	Spleen	Spleen
5	chr7:127991200-127993000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:127991400-127992800	Bivalent Enhancer	Brain Hippocampus Middle	brain
7	chr7:127991400-127992800	Enhancers	Gastric	stomach
8	chr7:127991400-127992800	Flanking Active TSS	Right Ventricle	heart
9	chr7:127991400-127993200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
10	chr7:127991800-127992800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
11	chr7:127991800-127992800	Enhancers	Placenta Amnion	Placenta Amnion
12	chr7:127992000-127992800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
13	chr7:127992200-127992800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
14	chr7:127992200-127992800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
15	chr7:127992200-127993000	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr7:127992200-127993200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr7:127992400-127992800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
18	chr7:127992400-127992800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:127992400-127992800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr7:127992400-127992800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
21	chr7:127992400-127992800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:127992400-127992800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:127992400-127992800	Bivalent Enhancer	Fetal Stomach	stomach
24	chr7:127992400-127992800	Enhancers	Pancreas	Pancrea
25	chr7:127992400-127992800	Bivalent Enhancer	Rectal Smooth Muscle	rectum
26	chr7:127992400-127992800	Genic enhancers	Right Atrium	heart
27	chr7:127992400-127993000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
28	chr7:127992400-127993000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr7:127992400-127993200	Bivalent Enhancer	Fetal Intestine Large	intestine
30	chr7:127992600-127992800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
31	chr7:127992600-127992800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:127992600-127992800	Bivalent Enhancer	Primary T cells from cord blood	blood
33	chr7:127992600-127992800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
34	chr7:127992600-127992800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr7:127992600-127992800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:127992600-127992800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:127992600-127992800	Enhancers	Adipose Nuclei	Adipose
38	chr7:127992600-127992800	Bivalent Enhancer	Fetal Brain Male	brain
39	chr7:127992600-127992800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
40	chr7:127992600-127992800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
41	chr7:127992600-127993000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
42	chr7:127992600-127993000	Bivalent Enhancer	Esophagus	oesophagus
43	chr7:127992600-127993000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
44	chr7:127992600-127993000	Bivalent Enhancer	HepG2	liver
45	chr7:127992600-127993000	Enhancers	K562	blood
46	chr7:127992600-127993200	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr7:127992600-127993800	Bivalent Enhancer	Fetal Heart	heart

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