Variant report

Variant	rs190031746
Chromosome Location	chr6:13713898-13713899
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr6:13713885-13714176	SH-SY5Y	brain:	n/a	chr6:13714130-13714151 chr6:13714134-13714144

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:13703743..13705757-chr6:13712344..13714353,2	MCF-7	breast:
2	chr6:13712256..13714398-chr6:13725384..13727195,2	MCF-7	breast:
3	chr6:13613792..13617654-chr6:13711804..13714048,3	K562	blood:
4	chr6:13712562..13715550-chr6:13731027..13734094,5	K562	blood:
5	chr6:13712294..13715235-chr6:13734842..13736345,2	K562	blood:
6	chr6:13658437..13687167-chr6:13707669..13717356,51	K562	blood:
7	chr6:13613655..13618769-chr6:13709987..13714197,10	MCF-7	breast:
8	chr6:13711887..13713957-chr6:13747635..13751147,3	K562	blood:
9	chr6:13667308..13669773-chr6:13712805..13714594,2	K562	blood:
10	chr6:13713710..13717343-chr6:13751875..13754798,3	MCF-7	breast:
11	chr6:13711847..13714774-chr6:13741208..13742857,2	K562	blood:
12	chr6:13677099..13683232-chr6:13708060..13717356,16	K562	blood:
13	chr6:13709898..13716469-chr6:13809605..13815390,11	K562	blood:

No data

Variant related genes	Relation type
RANBP9	TF binding region
ENSG00000050393	Chromatin interaction
ENSG00000261071	Chromatin interaction
ENSG00000225921	Chromatin interaction
ENSG00000252966	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532021	chr6:13232627-13805381	Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv883451	chr6:13704341-13728670	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
3	nsv883452	chr6:13704341-13733565	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
4	esv3404065	chr6:13709573-13714171	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
5	esv3352859	chr6:13713873-13716971	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13712800-13715600	Weak transcription	Esophagus	oesophagus
2	chr6:13712800-13715600	Weak transcription	Gastric	stomach
3	chr6:13712800-13716800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:13712800-13717000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:13713000-13716600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:13713200-13714000	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr6:13713200-13714000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:13713200-13714000	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr6:13713200-13714200	Enhancers	Colon Smooth Muscle	Colon
10	chr6:13713200-13715000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr6:13713200-13715200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr6:13713200-13715400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:13713200-13715400	Enhancers	Fetal Heart	heart
14	chr6:13713200-13716400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:13713400-13714000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:13713400-13714000	Enhancers	Dnd41	blood
17	chr6:13713400-13715600	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr6:13713400-13715800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:13713600-13715000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:13713600-13715000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr6:13713600-13715200	Weak transcription	GM12878-XiMat	blood
22	chr6:13713600-13715400	Weak transcription	HepG2	liver
23	chr6:13713600-13715600	Weak transcription	K562	blood
24	chr6:13713600-13715800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr6:13713600-13716000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr6:13713600-13717200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr6:13713800-13714000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr6:13713800-13715600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr6:13713800-13716000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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