Tag | Content |
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EnhancerAtlas ID | HS187-18883 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr4:122034530-122036210 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLTF | MA0109.1 | chr4:122035353-122035363 | AACCTTATAT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAAAATGTTA AATTTGGAAT ATGATAAACA TTTCAAAAGG ATGTTGGGAA TGTAAGAAGT 60 TCCATGACCC TGAAAATTGA TAGCAATGCT AGAATAAAAT ACTCCATCTG AGAAACCTTT 120 GCAAGTTCTC AAGCAACTAT GAATGTCATC CAGTGGTACA CTGGTGAACC TGATAATCTC 180 TTTTGCTGGA ATATTTTAAA ATTCAATTTC ACTTGAAGGA ACTGTTGATT GCAAATATGC 240 CATTAGTTTC TTCATATAAG ACAACAGATA AATCACCAAC ACTAGCTTTA TAATGCAGTC 300 AACATTCTGA AATACATTTA TTTCATATAA TAAAGACACT AAAATTTAGG CCAAATTTAA 360 AGTTCAAAGA ATAGCTTTGA AATAAGACCA TAGATGAGGG TCTAAGGTTC TGAAGGTCTA 420 AGGGATTAAG ATGTAGCCTA TGAATAGGCA AACCACTTCA AAAATGCCAA ATGATTGCTC 480 AAACTGAAAT CGTAGACTGA GGTTGGCAAA AGTGAGAACT GAAAACATCT AAGGTTGCAT 540 TACTACAGCA AACAACCAAG CCTGACTTAA AAATGTGCAG ATTGGCTGCT ATCATATTGC 600 TGAAGAGGCA GGCTTTTGAT TTTTAGTCAA AATGGCTTGG CCAACATGGA CACTTTATTG 660 TCACACATAA CTAGGGCTTC TGATGTAGGG AGGCGCCAGG ATTGATTGAT TCAGCAAATC 720 AAGAATGTCA TTAAGTATCC ACAGTCATTC TTTTTGTTCT ACCAGCCTTC AGCCTTGCTC 780 TTTTGTTACT CCTTTTCATG TTTGCAAAAT GACGTTATCT CCAAACCTTA TATCCTCATA 840 CATCAATGTC CAGAGACAAA ACAAAAAAAC AAAAGGGTGC TCCCTCTCTC TCTCTCTTTC 900 TCTCTCTCTC TCTCTCTCAC ACACACACAC ACACACACAC ATCTCTTTTT AAGAACTTGG 960 AATCTTTCCC CAAAAAATAC CCCATATATT TCAATGTCCA CTCATGTATT ACTACTTAGA 1020 ATTGGATCAG GAACCTCTTT GCAACCCAAC CTCAAACTGG CAAGGGAAAT GCAATTCCTG 1080 TACTGTGTTA TGATTGGTAG AGGATAATTA AGGTTCCATC TGGGCTGAGA CTAAAGCAGG 1140 ACTGGACTTC TCTGAGAACT CTAATAATAC CTGCATCAAA TATAAGTTCT ATAATAAGGA 1200 AACGGGCTCC TTGGGAAGAA AACCAAGTGT CTGCTACACA GCACAACATA AAGCAACAGA 1260 AATTGACATC ACGAAGGCCA ACAGAGAAAC TGTTAGCATG GAAGATACCA TGCTAAATAG 1320 AATGTATAAA TAAAAAAGAA ACACACTCAG AGGGGCTAAA GGAAGGAAAA ACATCGGAAG 1380 TATGCTTCCA TCTAATCCTT CTGTATCTGG AAACTTTATT TCTGACTCCA GACCACCCCA 1440 AGCAGTGGCA GCCTAACATC TTAGGGCCAC TTTTCACAGG GAGCGTATAC AAAAGTAGAA 1500 GAATGATAAT GACTTGCTCT GCAGAATAGT GGGAGAGCAA AAGGGTTTTG TTCTGACTGC 1560 ATCTTTCCCC ACCATAATTC TGTGGGTTCT TTATGCTTAC ACATACACAA CTCATGCAGG 1620 CTCTATCTAA CCTTGCTGTG TGGCTGATTC TGGAGTTGTT TTATCCTGTG AGAGGAGGGC 1680
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