Tag | Content |
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EnhancerAtlas ID | HS053-26034 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr22:42551820-42553300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr22:42552753-42552768 | ACTGCTGTGTCATGG | - | 6.11 | Nfe2l2 | MA0150.2 | chr22:42552755-42552770 | TGCTGTGTCATGGTA | - | 6.34 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GATCCTATTT TAGCGTCCCG AGTAGCTGGA ACTACAGGTG CACATCATTA CGCTCGGCTA 60 ATTTTTTTGT TGAGATGGGT CCTCACTATG TTGCCCACGC TGGTCTGGAA CTCCTGGCTT 120 CAAGTGATCC TCCTGCCTTG GCCTCCCAAA GTGTTGGAAA TAGAGGCATG AGCCACCTGG 180 CCCAACAGAA GTTTTGAAGC TACTCAACTG ACAGAGAGAG CAAGACCCAT GCCTATCTGG 240 GGACTTCTCA GATCTGGCTT GTGGTCTCCC AAACTGGCCT CAGCTGAATG AATGTTCCTG 300 TCCTACATGG CAGCACTGTT CTATTTGGGA CTGTGAGAGA ATCAAGGTGC AGGGACAGCA 360 GGATGGTCTG GGTGCTTGTT ACATGGTGGC CCTTTATACA TTACCTGTAT GCACTCTTGG 420 CCTTTTGAGG TGTCAGGCCC TCCCCAAGCA GTCATCATGA ATCATGATGG GGGTGTGAAG 480 GGCAGGGACA GGCATGCCTG CAATGTGGGC AGTGTCCTCC CGAGTGCCCT CCTTACCAGC 540 CAGAGGCCTG TAATTCAAGA TATGGCAGCA TGAGGAAAAC ATTTAATAAC AATGCCTGTG 600 GCCTTTTCCA ATCATTGTGC ACCTGTGGCT TCCATTGATC GGGCACTTAT GTGCCAGAAA 660 CTGCTGGTCA GACTGTGTGC TCTAGCTCAT TAATCCTCCC ACAGCCCCCT AAGGAGGTGG 720 TTTTATGGTC CCCAAGGCAC AGAGACTGAG GCTCAGAGAT CACATAACAA GGTTCAAGTC 780 ACACAGCGGT GTTAGGAGTC CACATCCAAT GTGTATGCTG AGCTACTATT CTATACTGTT 840 TGGACATTAC ATTCTATTAA TGGTCAGTAT AGATGTTTCT GGGATTTATT ATTTTTAGGA 900 AACAGATCCA ACCTGCCTTC CCTGAACAGT GGTACTGCTG TGTCATGGTA AAAAGTGCAC 960 TGTGCCCTGG CAGGCCCTAT GGACGTTGCC AAGTGAGATG GTGTGAAAAT ATGTCAGCAA 1020 GTGGTAGACT AGGAAACTGC GGGCTCTCGT TCTCTTAGAG AGCTCAATGT TAAAGCTATA 1080 GGAGACCAAA ACATCGTGAG AATTCTAGAA ACTAGTTAGG ATGCTGCAAT GCCAGCTAGT 1140 GCAGAGCCAG GGAGGGACTG CACTGGGAAG GGTAGTCAAG TTGGAGCATT TTGCTTGTTC 1200 TTGCCCTTCC CCCTGCCAGG CATAGCAATG CTACTGGGAG AGACCCTCCA ATTCCCAGCT 1260 CCTCCCATGG GATGGGTTTC TGCTGGGTCC GACTCAAGAG TGCTGAGTGG TGGGGTCTGT 1320 CTGCCCTCAG AGCAGCACCT CTGCGTTTCC ACAGCTGCAA GGGGACGGGG TTATGGGCAG 1380 TGGAATAGTT GTGTCTGGGT ATCCTGGAGG GGATTGGTGC CAGGACCCCC GGTAAATACC 1440 AAAACCCAAG GATGCTCAGG TTCCTTATGT AAAATGGCAT 1480
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