Variant report

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:98807413-98810111	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr7:98808713-98810062	HepG2	liver:	n/a	n/a
3	TCF12	chr7:98808859-98809942	A549	lung:	n/a	chr7:98809542-98809549

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:98721425..98723767-chr7:98806465..98809403,2	MCF-7	breast:
2	chr7:98758729..98762342-chr7:98808089..98809747,3	MCF-7	breast:
3	chr7:98807183..98812417-chr7:98813436..98818450,10	MCF-7	breast:
4	chr7:98807265..98810785-chr7:98821071..98827725,5	MCF-7	breast:
5	chr7:98702195..98704241-chr7:98806871..98809621,2	MCF-7	breast:
6	chr7:98679090..98681907-chr7:98808014..98810256,2	MCF-7	breast:
7	chr7:98797515..98801446-chr7:98806232..98810784,4	MCF-7	breast:
8	chr7:98807837..98811719-chr7:98828623..98830666,3	MCF-7	breast:
9	chr7:98694785..98697794-chr7:98808193..98811176,3	MCF-7	breast:
10	chr7:98762592..98764850-chr7:98807943..98809582,2	MCF-7	breast:
11	chr7:98738526..98746153-chr7:98804876..98809686,18	MCF-7	breast:
12	chr7:98808636..98811320-chr7:98812026..98815181,4	MCF-7	breast:
13	chr7:98807843..98809841-chr7:98921913..98924740,2	MCF-7	breast:
14	chr7:98807571..98809219-chr7:98875910..98878236,2	MCF-7	breast:
15	chr7:98803072..98806068-chr7:98806546..98809669,4	MCF-7	breast:
16	chr7:98740103..98745000-chr7:98806658..98810214,11	MCF-7	breast:
17	chr7:98808174..98810651-chr7:98856542..98858905,3	MCF-7	breast:

No data

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1004387	1.00[AFR][1000 genomes]
rs12705053	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13228146	1.00[AFR][1000 genomes]
rs13230554	1.00[AFR][1000 genomes]
rs13234987	1.00[AFR][1000 genomes]
rs35392648	1.00[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3433144	chr7:98777878-99060209	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98802600-98823400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:98804800-98809600	Enhancers	Fetal Intestine Small	intestine
3	chr7:98805000-98811400	Enhancers	Fetal Intestine Large	intestine
4	chr7:98805400-98809800	Enhancers	Placenta	Placenta
5	chr7:98805400-98811400	Enhancers	Pancreas	Pancrea
6	chr7:98806400-98809600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:98806800-98809200	Enhancers	Liver	Liver
8	chr7:98807400-98809800	Enhancers	HMEC	breast
9	chr7:98807600-98809600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:98807600-98809600	Enhancers	Duodenum Mucosa	Duodenum
11	chr7:98807600-98809800	Enhancers	NHEK	skin
12	chr7:98807600-98810000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:98807800-98809400	Enhancers	Placenta Amnion	Placenta Amnion
14	chr7:98808000-98809200	Enhancers	Hela-S3	cervix
15	chr7:98808200-98809000	Enhancers	HepG2	liver
16	chr7:98808200-98809200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:98808400-98809000	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr7:98808400-98809000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr7:98808400-98809400	Enhancers	Colonic Mucosa	Colon
20	chr7:98808400-98809400	Enhancers	Esophagus	oesophagus
21	chr7:98808400-98811600	Enhancers	Stomach Mucosa	stomach
22	chr7:98808600-98809000	Enhancers	A549	lung

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