Variant report

Variant	rs140188327
Chromosome Location	chr7:138333769-138333770
allele	A/G
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	CTCF	chr7:138333720-138333870	BE2_C	brain:	n/a	n/a
2	CTCF	chr7:138333761-138333843	MCF-7	breast:	n/a	n/a
3	ZNF143	chr7:138333711-138333954	H1-hESC	embryonic stem cell:	n/a	n/a
4	RAD21	chr7:138333727-138333872	HepG2	liver:	n/a	n/a
5	CTCF	chr7:138333683-138333919	K562	blood:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
6	CTCF	chr7:138333740-138333890	HRPEpiC	eye:	n/a	n/a
7	CTCF	chr7:138333609-138333901	H1-hESC	embryonic stem cell:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
8	CTCF	chr7:138333700-138333850	K562	blood:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
9	RAD21	chr7:138333712-138333868	HepG2	liver:	n/a	n/a
10	CTCF	chr7:138333612-138333948	K562	blood:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
11	CTCF	chr7:138333720-138333906	K562	blood:	n/a	n/a
12	CTCF	chr7:138333680-138333830	K562	blood:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
13	CTCF	chr7:138333700-138333850	Hela-S3	cervix:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
14	CTCF	chr7:138333700-138333850	MCF-7	breast:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
15	CTCF	chr7:138333740-138333891	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr7:138333760-138333910	GM12872	blood:	n/a	n/a
17	RCOR1	chr7:138333693-138333933	K562	blood:	n/a	n/a
18	CTCF	chr7:138333680-138333830	WERI-Rb-1	eye:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
19	CTCF	chr7:138333720-138333870	HEK293	kidney:	n/a	n/a
20	RAD21	chr7:138333553-138334032	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr7:138333720-138333870	HepG2	liver:	n/a	n/a
22	RAD21	chr7:138333622-138333932	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr7:138333696-138333910	MCF-7	breast:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
24	RAD21	chr7:138333626-138333977	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:138333696-138333874	HepG2	liver:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
26	CTCF	chr7:138333680-138333830	SK-N-SH_RA	brain:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
27	CTCF	chr7:138333720-138333870	GM06990	blood:	n/a	n/a
28	CTCF	chr7:138333720-138333870	GM12875	blood:	n/a	n/a
29	CTCF	chr7:138333740-138333890	GM12873	blood:	n/a	n/a
30	CTCF	chr7:138333732-138333871	Gliobla	brain:	n/a	n/a
31	CTCF	chr7:138333740-138333876	MCF-7	breast:	n/a	n/a
32	RAD21	chr7:138333715-138333870	K562	blood:	n/a	n/a
33	CTCF	chr7:138333749-138333849	GM12891	blood:	n/a	n/a
34	CTCF	chr7:138333720-138333870	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr7:138333700-138333850	BE2_C	brain:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
36	CTCF	chr7:138333644-138333901	H1-hESC	embryonic stem cell:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
37	CTCF	chr7:138333735-138333853	MCF-7	breast:	n/a	n/a
38	RAD21	chr7:138333674-138334012	HCT-116	colon:	n/a	n/a
39	RAD21	chr7:138333711-138333921	K562	blood:	n/a	n/a
40	CTCF	chr7:138333660-138333810	SK-N-SH_RA	brain:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
41	CTCF	chr7:138333700-138333850	A549	lung:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
42	CTCF	chr7:138333762-138333886	GM12878	blood:	n/a	n/a
43	CTCF	chr7:138333699-138333918	H1-hESC	embryonic stem cell:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
44	CTCF	chr7:138333540-138334058	K562	blood:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
45	CTCF	chr7:138333756-138333850	MCF-7	breast:	n/a	n/a
46	JUND	chr7:138333741-138333918	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr7:138333648-138333986	K562	blood:	n/a	chr7:138333712-138333725 chr7:138333709-138333727
48	SMC3	chr7:138333752-138333907	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:138134483..138135008-chr7:138333376..138334299,2	K562	blood:

Variant related genes	Relation type
ENSG00000234658	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	nsv1030956	chr7:138163169-138579519	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription 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	19 gene(s)	inside rSNPs	diseases
2	esv3438653	chr7:138333736-138336496	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138330200-138333800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:138333600-138335200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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