Variant report

Variant	rs191038637
Chromosome Location	chr9:136779181-136779182
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:136727889..136730312-chr9:136777373..136780335,2	MCF-7	breast:
2	chr9:136776944..136779401-chr9:136782904..136785015,2	MCF-7	breast:
3	chr9:136772619..136776422-chr9:136776725..136781488,5	K562	blood:
4	chr9:136779162..136780728-chr9:136807487..136809424,2	MCF-7	breast:
5	chr9:136737105..136739674-chr9:136778546..136781444,2	MCF-7	breast:
6	chr9:136777667..136779284-chr9:136788420..136790198,2	K562	blood:
7	chr9:136776480..136779233-chr9:136856676..136858268,2	MCF-7	breast:
8	chr9:136747009..136748873-chr9:136778099..136780165,2	MCF-7	breast:
9	chr9:136757643..136759941-chr9:136779061..136782245,3	MCF-7	breast:
10	chr9:136775409..136777702-chr9:136777760..136779303,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000160293	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831745	chr9:136593702-136780273	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv894123	chr9:136682408-136852501	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv894124	chr9:136716399-136870787	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv894125	chr9:136723520-136931957	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv894127	chr9:136747832-136811772	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv1832030	chr9:136753246-136785840	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv1829795	chr9:136753246-136787253	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv894128	chr9:136753246-136906752	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS 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	25 gene(s)	inside rSNPs	diseases
9	nsv615739	chr9:136761938-136790282	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv466625	chr9:136762800-136787972	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv615740	chr9:136762800-136787972	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv1046310	chr9:136762829-136872226	Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
13	nsv894130	chr9:136767346-136906752	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
14	esv3422697	chr9:136778731-136783129	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	esv3412806	chr9:136778981-136780979	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136729600-136780000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr9:136747600-136780800	Weak transcription	Right Atrium	heart
3	chr9:136753000-136813200	Weak transcription	Aorta	Aorta
4	chr9:136758400-136781000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr9:136758800-136780000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:136763200-136780800	Weak transcription	Hela-S3	cervix
7	chr9:136765800-136797200	Weak transcription	HSMMtube	muscle
8	chr9:136766600-136784400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr9:136771000-136780800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:136772600-136782200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:136772800-136779200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:136772800-136780000	Weak transcription	NHLF	lung
13	chr9:136772800-136780400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:136773600-136779200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:136774800-136802000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:136776600-136780000	Weak transcription	Ovary	ovary
17	chr9:136776800-136780800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr9:136777000-136779400	Weak transcription	Fetal Lung	lung
19	chr9:136777000-136780000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:136777000-136780000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr9:136777000-136780000	Weak transcription	Esophagus	oesophagus
22	chr9:136777000-136780000	Weak transcription	Gastric	stomach
23	chr9:136777000-136780200	Weak transcription	Stomach Mucosa	stomach
24	chr9:136777000-136780600	Weak transcription	HMEC	breast
25	chr9:136777000-136783200	Enhancers	Fetal Brain Female	brain
26	chr9:136777000-136786200	Weak transcription	NHEK	skin
27	chr9:136777200-136779800	Genic enhancers	HepG2	liver
28	chr9:136777200-136780800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr9:136777200-136780800	Enhancers	Brain Cingulate Gyrus	brain
30	chr9:136777400-136780800	Enhancers	Fetal Brain Male	brain
31	chr9:136777600-136780000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr9:136777600-136780000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:136777600-136781800	Enhancers	Liver	Liver
34	chr9:136777600-136786400	Weak transcription	Primary B cells from cord blood	blood
35	chr9:136777800-136780200	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr9:136777800-136781200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr9:136777800-136796600	Weak transcription	HUVEC	blood vessel
38	chr9:136778000-136779400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr9:136778000-136780600	Enhancers	Brain Hippocampus Middle	brain
40	chr9:136778000-136781000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr9:136778000-136781600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr9:136778000-136785800	Enhancers	Fetal Muscle Leg	muscle
43	chr9:136778000-136791200	Weak transcription	GM12878-XiMat	blood
44	chr9:136778200-136779200	Weak transcription	Brain Angular Gyrus	brain
45	chr9:136778200-136780000	Weak transcription	Spleen	Spleen
46	chr9:136778200-136780800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr9:136778400-136779400	Strong transcription	Primary B cells from peripheral blood	blood
48	chr9:136778400-136780800	Enhancers	Pancreas	Pancrea
49	chr9:136778400-136781400	Enhancers	Lung	lung
50	chr9:136778600-136779400	Strong transcription	Fetal Stomach	stomach

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