Variant report

Variant	rs181582003
Chromosome Location	chr7:96647236-96647237
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	chr7:96629453-96654775	H1-neurons	neurons:	n/a	n/a
2	EBF1	chr7:96647058-96647493	GM12878	blood:	n/a	chr7:96647251-96647261 chr7:96647265-96647276 chr7:96647250-96647261
3	CTBP2	chr7:96645669-96647906	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr7:96647155-96647543	HepG2	liver:	n/a	n/a
5	SUZ12	chr7:96645469-96648990	H1-hESC	embryonic stem cell:	n/a	n/a
6	REST	chr7:96645097-96647724	H1-neurons	neurons:	n/a	n/a
7	POLR2A	chr7:96628026-96649797	H1-neurons	neurons:	n/a	n/a
8	REST	chr7:96624507-96656402	H1-neurons	neurons:	n/a	chr7:96626900-96626913 chr7:96628274-96628287 chr7:96653242-96653252 chr7:96638441-96638449 chr7:96644780-96644790 chr7:96627625-96627635 chr7:96628223-96628236 chr7:96655951-96655958 chr7:96625513-96625526 chr7:96635204-96635222 chr7:96634677-96634690 chr7:96628302-96628315 chr7:96652071-96652084 chr7:96650634-96650647 chr7:96628298-96628318 chr7:96628298-96628318
9	SUZ12	chr7:96645885-96648969	NT2-D1	testis:	n/a	n/a
10	EBF1	chr7:96647146-96647393	GM12878	blood:	n/a	chr7:96647251-96647261 chr7:96647265-96647276 chr7:96647250-96647261

Variant related genes	Relation type
DLX6-AS1	TF binding region

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv824221	chr7:96620279-96669211	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3337466	chr7:96647166-96649364	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96644600-96648200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:96645200-96647800	Flanking Active TSS	Osteobl	bone
3	chr7:96645200-96651600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr7:96645400-96648400	Bivalent Enhancer	Fetal Brain Male	brain
5	chr7:96645600-96647400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
6	chr7:96645600-96647400	Bivalent Enhancer	Brain Substantia Nigra	brain
7	chr7:96645600-96647800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:96645600-96647800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr7:96645600-96647800	Bivalent Enhancer	Fetal Stomach	stomach
10	chr7:96645600-96647800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
11	chr7:96645600-96648200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr7:96645800-96647400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:96645800-96648200	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr7:96646200-96647800	Bivalent Enhancer	Psoas Muscle	Psoas
15	chr7:96646400-96647400	Bivalent Enhancer	Spleen	Spleen
16	chr7:96646400-96647600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:96646400-96648000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
18	chr7:96646400-96648000	Bivalent Enhancer	Esophagus	oesophagus
19	chr7:96646600-96647400	Bivalent Enhancer	Placenta	Placenta
20	chr7:96646600-96647600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:96646600-96647600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
22	chr7:96646600-96647800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:96646600-96648000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr7:96646600-96648000	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr7:96646600-96648000	Enhancers	Right Atrium	heart
26	chr7:96646600-96648200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:96646800-96647400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
28	chr7:96646800-96647400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
29	chr7:96646800-96647600	Bivalent Enhancer	Brain Hippocampus Middle	brain
30	chr7:96646800-96647800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:96646800-96647800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:96646800-96648000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:96646800-96648000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:96646800-96648000	Bivalent Enhancer	Right Ventricle	heart
35	chr7:96647000-96647400	Bivalent Enhancer	Colonic Mucosa	Colon
36	chr7:96647000-96647400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
37	chr7:96647000-96647400	Weak transcription	Pancreas	Pancrea
38	chr7:96647000-96647600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
39	chr7:96647000-96650200	Bivalent/Poised TSS	Fetal Brain Female	brain
40	chr7:96647000-96655200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
41	chr7:96647200-96647400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
42	chr7:96647200-96647400	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
43	chr7:96647200-96647400	Bivalent Enhancer	Colon Smooth Muscle	Colon
44	chr7:96647200-96647800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
45	chr7:96647200-96647800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr7:96647200-96647800	Enhancers	HepG2	liver

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