Tag | Content |
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EnhancerAtlas ID | HS108-22952 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:102636990-102637940 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:102637247-102637266 | TGAACACTAGGGGGCAGCC | + | 6.49 | ZNF263 | MA0528.1 | chr2:102637545-102637566 | GGAGGAGGGGAGGAAAAGGCG | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_44807 | chr2:102636977-102637643 | NHLF | SE_45585 | chr2:102634481-102639286 | Osteoblasts | SE_52672 | chr2:102637135-102637955 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I102020 | chr2 | 102636681 | 102637862 |
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Enhancer Sequence | GGGGATTTCA GAGAGCTTCA GAGACACGCT AAGTTTAAAT AATTGGTCTA TAAGGGGAAA 60 ATATATTTTT CTCACAGAGC ATCCAGAGAT TCAGTTGCAC CGCATTTTCC CACGGACTGA 120 GGTGTCCTGA TTGTGTTTGT TTTACAGTCC TGTGAGGATT CGTTCATATC AGCTCCTTGC 180 TTCTGGACAG GCCACTGACT CAGGTCTCCT GAGGCTTTCC GTGGACCGGC ACGGTCCTGT 240 CTCTGCGATA CTGTGCATGA ACACTAGGGG GCAGCCGCCC TACATGCCTG TCTGTGTTGT 300 GATCCTCCCA GGATCTCAGT GGCTCTCAAG GGGTGGTCCT GGGCCAGCAG CGCCTCATCA 360 CCTGGGTACT CAACAGACAT GCAAATCTCG GGTCCCGTGG AGACCTACTG ATTGAAACTG 420 GAGTCTGGGG GCTGTCATCT GTGTCTCACA AGCCCCCGGG TGATGCTGGG GACCCTCAAG 480 TCTAAGAAGC ACTGAGATCC TGGAGGCTTC TTTCTCTCCC TGGATGCCCC AGCTCCATAG 540 GGCAGCGCGT GACTTGGAGG AGGGGAGGAA AAGGCGTCTG GCCGTGGTCG AAAAGCCGTC 600 TGCCCCTCAG GCTGTCCTGC CATGCTGTCT AATGTGTACT CATGTCAGGA TTTCAAAATG 660 CTGTTTCGTG GAAGTGAGGA TGATGAGGCC CGTCGTGGAG ACAACTCACA GCCCTCACCC 720 CCCAGGTGTC CTTTTTGCTC ATTTCAGGGG CCTCGTTTCT TTCTTTCTTT TCTTTTCTTT 780 TTTTTTTTTT TTTTGGTTTT TTTTTGAGGC GGAGTCTCGC TCTGCCACCC AGGCTGGAGT 840 GCAATGGCGC GATCTCGGCT CACTGCGACC TCTACCTCCC GGGTTCAAGC GATTATCCTG 900 TCTCAGCCTC CTGAGTAGCT GGGATTACAG GCTTACGCCA CCAAGCCCAG 950
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