Variant report

Variant	rs6970366
Chromosome Location	chr7:16833075-16833076
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16831486..16833209-chr7:16838972..16841146,2	K562	blood:
2	chr7:16829911..16832805-chr7:16833008..16837157,5	MCF-7	breast:
3	chr7:16832562..16837080-chr7:16918023..16922699,4	MCF-7	breast:
4	chr7:16816860..16820045-chr7:16832794..16835975,4	MCF-7	breast:
5	chr7:16832553..16834809-chr7:16849103..16850683,2	MCF-7	breast:
6	chr7:16806775..16809760-chr7:16831007..16833203,2	K562	blood:

Variant related genes	Relation type
ENSG00000106541	Chromatin interaction
ENSG00000173467	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs13242497	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1997116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2272246	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781662	0.81[ASN][1000 genomes]
rs7796640	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs898286	0.87[ASN][1000 genomes]
rs940827	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028125	chr7:16529160-16847225	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1024059	chr7:16639432-16836425	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16811400-16833600	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:16814000-16834600	Weak transcription	Fetal Brain Male	brain
3	chr7:16814400-16843800	Weak transcription	Small Intestine	intestine
4	chr7:16815000-16838000	Weak transcription	K562	blood
5	chr7:16816800-16835000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:16819800-16838000	Weak transcription	Placenta	Placenta
7	chr7:16820200-16835400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:16823600-16835400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr7:16823600-16843600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:16825800-16833600	Weak transcription	Gastric	stomach
11	chr7:16825800-16834400	Weak transcription	Fetal Brain Female	brain
12	chr7:16825800-16834600	Weak transcription	Fetal Stomach	stomach
13	chr7:16825800-16836600	Weak transcription	Left Ventricle	heart
14	chr7:16827400-16837000	Weak transcription	Primary B cells from cord blood	blood
15	chr7:16827600-16835400	Weak transcription	Stomach Mucosa	stomach
16	chr7:16828000-16834400	Weak transcription	Fetal Intestine Small	intestine
17	chr7:16830800-16834400	Weak transcription	HSMMtube	muscle
18	chr7:16831400-16833600	Weak transcription	A549	lung
19	chr7:16831600-16833200	Weak transcription	Colonic Mucosa	Colon
20	chr7:16831800-16839200	Strong transcription	Placenta Amnion	Placenta Amnion
21	chr7:16832000-16835600	Strong transcription	Fetal Intestine Large	intestine
22	chr7:16832000-16839600	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr7:16832200-16833200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr7:16832200-16833800	Strong transcription	Duodenum Mucosa	Duodenum
25	chr7:16832400-16838200	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr7:16832400-16840000	Strong transcription	Rectal Mucosa Donor 29	rectum

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