Tag | Content |
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EnhancerAtlas ID | HS092-10616 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:119106820-119108100 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr11:119107660-119107673 | GAAAATTCTAGAA | - | 6.71 | NFAT5 | MA0606.1 | chr11:119107656-119107666 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr11:119107656-119107666 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr11:119107656-119107666 | AATGGAAAAT | - | 6.02 | NFE2L1 | MA0089.2 | chr11:119107347-119107362 | ATTGCTGAGTCATAT | - | 7.68 | Nfe2l2 | MA0150.2 | chr11:119107349-119107364 | TGCTGAGTCATATGG | - | 6.37 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I119237 | chr11 | 119107761 | 119107910 |
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Enhancer Sequence | TAGTGGTTTT TAGTGTATTC GCAAAGTCAG GCAACCATCA CCCCTCTGTA ATTCCAGAAC 60 ATTTTCACCC CCCAACAGGA AACCCCACTC CCATTAGCAG TCACTCTTTG TTCCTCTCTC 120 TGGATCTCCC CTGGCGCTTG GTAATCACTA ATACCTGCTT TCTGTCTATG TGGATTTGCC 180 TGCTCTGGAC GTTTCGTGTT AAGTGGAATC ACATAACGGT GGCCTTTTGT GGTTTTTTTT 240 TGTGTGTCTT CTTTCGCTTA GAATGTTTTT ACAATTCACC CATATTGTAG CATGTATTGG 300 TACCTCATTC CTTTTTATGG CTAAGTCATA TTTCAATGTA TGGATATACC ATATTTTGTT 360 TATGATATTT TTGTCATTTC TACTTTTTGG CTACTACTGA ATAATGTTGC TATGATTATG 420 TGCCAGTTTT TGTATGGCTA TAGCCATATA AACATATATA CATATATGTT TTCACTTCTT 480 TTGAGTATAT ATATATATAT ATATATATAT ATACCCATAG GAGTGGAATT GCTGAGTCAT 540 ATGGTAATTC TGTGTTCAAC TTTTGAGTAA CCTCCAAACT ATTTCCACAG TAGCTGTACC 600 ATTTTTCTTT CCCCTAGCAA TGTATGTGGG TTCTGATTTT TTGCTAACAA TTGCTATTGA 660 CTTTTTTTAT TACAGCTATT CTACTAGGGG TAAAGTGGTG TCTTGAGGTT TTGAAATGCA 720 TGTGAATACT TTTTCATGTG CCTCTTGGAT GTTTGTATAT AGTTGTCCCC CTTTATCCTC 780 AGTTTAACCT TCCTTGGATT CAGTTACTGG CAGTCAACCA TGGTTTGAAA ATATTAAATG 840 GAAAATTCTA GAAATAATTC ATAAATTTTG AATTGCATGC CCTTCAGAGT AGTGTGATGT 900 AATTTCACAA CGTTCTACTT TATCCCAGCT GGGATGCAAA GCATCCCTTT GTACAGCATC 960 TCCATGCTGT ATACACTAGC ACCTATTAGT CACCTAGTAG CTATCTTAGT TATCAGAGTG 1020 AGAAAACATA ATATACACAG GGTTCAGTAC TATCTGTGGT TTCAGGCATC TGCACATCTT 1080 GGAATGCAAA GGGGGACTAT TTATCTTCTT TGGAGAAACA TCTATTCAAA TCCTTTGCCC 1140 ATTTTAAAGT TGCATTATTT GTCTTTTCAT TGTTGAGTTG TAAGATTTTC CTTCATATTC 1200 TGGATGCTAG ACCAGATACA TGATTTGCAA AACTTTACTC CCATTCTGTG GGTCATCTTT 1260 TCACTTTCTT AACAGTATGC 1280
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