Variant report

Variant	rs140986092
Chromosome Location	chr4:187185729-187185730
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187185716-187185766	HCPEpiC	choroid plexus:	n/a
2	chr4:187185716-187185766	AG10803	skin:	n/a
3	chr4:187185716-187185766	HNPCEpiC	eye:	n/a
4	chr4:187185716-187185766	HUVEC	blood vessel:	n/a
5	chr4:187185716-187185766	HEEpiC	esophagus:	n/a
6	chr4:187185716-187185766	HCM	heart:	n/a
7	chr4:187185716-187185766	SKMC	muscle:	n/a
8	chr4:187185716-187185766	AG04450	lung:	fetal
9	chr4:187185716-187185766	HepG2	liver:	n/a
10	chr4:187185716-187185766	HCT-116	colon:	n/a
11	chr4:187185716-187185766	IMR90	lung:	fetal
12	chr4:187185716-187185766	PrEC	prostate:	n/a
13	chr4:187185716-187185766	NH-A	brain:	n/a
14	chr4:187185716-187185766	Hela-S3	cervix:	n/a
15	chr4:187185716-187185766	Hepatocyte	liver:	n/a
16	chr4:187185716-187185766	ovcar-3	ovarian:	n/a
17	chr4:187185716-187185766	NHDF-neo	bronchial:	n/a
18	chr4:187185716-187185766	HAEpiC	amniotic membrane:	n/a
19	chr4:187185716-187185766	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:187185716-187185766	A549	lung:	n/a
21	chr4:187185716-187185766	AG04449	skin:	fetal
22	chr4:187185716-187185766	SK-N-SH_RA	brain:	n/a
23	chr4:187185716-187185766	HEK293	kidney:	embryo
24	chr4:187185716-187185766	PFSK-1	brain:	n/a
25	chr4:187185716-187185766	NB4	blood:	n/a
26	chr4:187185716-187185766	RPTEC	kidney:	n/a
27	chr4:187185716-187185766	BE2_C	brain:	n/a
28	chr4:187185716-187185766	U87	brain:	n/a
29	chr4:187185716-187185766	SK-N-MC	brain:	n/a
30	chr4:187185716-187185766	Caco-2	colon:	n/a
31	chr4:187185716-187185766	HMEC	breast:	n/a
32	chr4:187185716-187185766	PANC-1	pancreas:	n/a
33	chr4:187185716-187185766	Jurkat	blood:	n/a
34	chr4:187185716-187185766	NHBE	bronchial:	n/a
35	chr4:187185716-187185766	AoSMC	blood vessel:	n/a
36	chr4:187185716-187185766	K562	blood:	n/a
37	chr4:187185716-187185766	SK-N-SH	brain:	n/a
38	chr4:187185716-187185766	HRPEpiC	eye:	n/a
39	chr4:187185716-187185766	ProgFib	skin:	n/a
40	chr4:187185716-187185766	NT2-D1	testis:	n/a
41	chr4:187185716-187185766	GM12891	blood:	n/a
42	chr4:187185716-187185766	HCF	heart:	n/a
43	chr4:187185716-187185766	GM12892	blood:	n/a
44	chr4:187185716-187185766	H1-hESC	embryonic stem cell:	embryo
45	chr4:187185716-187185766	SAEC	small airway:	n/a
46	chr4:187185716-187185766	GM12878	blood:	n/a
47	chr4:187185716-187185766	HRCEpiC	kidney:	n/a
48	chr4:187185716-187185766	GM19239	blood:	n/a
49	chr4:187185716-187185766	AG09319	gingival:	n/a
50	chr4:187185716-187185766	MCF10A-Er-Src	breast:	n/a

No data

Variant related genes	Relation type
F11	CpG island

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028146	chr4:186503899-187338335	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv530178	chr4:186659940-187478310	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv931977	chr4:186912987-187364756	Active TSS Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv869299	chr4:186958290-187192748	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1033203	chr4:186990348-187333476	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv537431	chr4:186990348-187333476	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv461864	chr4:187006806-187257004	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv596392	chr4:187006806-187257004	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv461865	chr4:187072383-187366649	Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv596401	chr4:187072383-187366649	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
11	nsv881472	chr4:187152142-187187005	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1034638	chr4:187185385-187213477	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187149800-187186800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:187150200-187187200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr4:187151000-187187200	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:187177400-187191800	Weak transcription	Right Atrium	heart
5	chr4:187180200-187185800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:187182200-187186000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:187182200-187187600	Weak transcription	Fetal Lung	lung
8	chr4:187182400-187185800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:187182600-187186000	Weak transcription	Fetal Intestine Large	intestine
10	chr4:187183000-187186000	Weak transcription	Pancreas	Pancrea
11	chr4:187184000-187186800	Enhancers	Liver	Liver
12	chr4:187185200-187186800	Enhancers	HepG2	liver
13	chr4:187185200-187187000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr4:187185400-187186200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:187185400-187186400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:187185400-187187000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr4:187185400-187187000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:187185600-187186000	Weak transcription	Fetal Intestine Small	intestine
19	chr4:187185600-187186800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:187185600-187186800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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