Variant report

Variant	rs4266301
Chromosome Location	chr4:98110950-98110951
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1002766	chr4:98006688-98128416	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv537192	chr4:98006688-98128416	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2653918	chr4:98110206-98111718	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv8786	chr4:98110366-98111159	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2287575	chr4:98110466-98111180	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3465779	chr4:98110525-98111070	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3528125	chr4:98110535-98111059	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3528128	chr4:98110551-98111025	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3528126	chr4:98110553-98111080	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3528124	chr4:98110573-98111003	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3465777	chr4:98110579-98111041	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3465780	chr4:98110585-98111036	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3528127	chr4:98110586-98111020	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3465778	chr4:98110591-98110994	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3465781	chr4:98110631-98110975	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3528123	chr4:98110643-98110970	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	nsv289695	chr4:98110645-98110970	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv3465782	chr4:98110645-98110984	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3528130	chr4:98110645-98110984	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98110400-98111200	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr4:98110400-98114800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:98110800-98111400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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