Tag | Content |
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EnhancerAtlas ID | HS077-00086 | Organism | Homo sapiens | Tissue/cell | H128 | Coordinate | chr1:7710570-7711470 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr1:7710632-7710644 | TGCCCCCTGGCA | - | 6.62 | MYC | MA0147.3 | chr1:7711073-7711085 | AGGCACGTGGCC | - | 6.07 | RFX1 | MA0509.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | + | 6.17 | RFX1 | MA0509.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | - | 6.19 | RFX2 | MA0600.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | + | 6.38 | RFX2 | MA0600.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | - | 6.3 | RFX5 | MA0510.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | - | 6.14 | RFX5 | MA0510.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | + | 6.28 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTCTGCTGG ACCCTCCACC CCCGCCTTTT CCAGAGGACG TGTGATGTTG GGACGAAGCC 60 CATGCCCCCT GGCAGAGGGA GGACTGTGAT GCCCCAACAG CGAGCACCAG AAATGACAGG 120 CTCACTGGGG ACACGGCAGA TAGGTCCCCG CATGTGCACA CGGTGGGCGC ACACTCCATC 180 CCGTCCCCCC TCAGCCTCTG CGCTCCTCGA AATGAGATTT CTGAAAATTT TGTCCTCAGG 240 ACCAATAGGC GAATGAGAGT TGAGTGGTGA GATCGGGAAA TTGAATAGTA TGTGGGTGTC 300 TGGATATGAG AAGTTAAATC TAATGAAAAT TTCATCCAGT TGAACCAAGA AATCAGAAAC 360 AGGGCCTTTA TTCCTGTCAA CAAGAATACA GTGAAAATTA AACCAACCCG GCTGCCATTT 420 CCCATTGACC TTGTCGCCAT GGAGACAGCC TTCTAGTGTC AACAACACCG AGGACTCCGA 480 AGGGGCCTCA TTCACTCCAG GAGAGGCACG TGGCCGCTCC CTCTCCCGTC CGCCTCCGGC 540 ACGTGGTTCA TAAGGAGAGC AGCCACACGT CCAGGGTTGC TGGAGAGCAA CCCAGCCTAT 600 ACCAGCACCT GGACAAATGA CCACAGCACC CTTTGTTGGC TCCCAAGGTG ACCTGGCTTG 660 ACTAGTTAAA TGGCCACCCT CTTTCTGGGT CTTTCTTGGG TGGCAGGGTA CCTAGGTGGG 720 TGGACTGGAC GAGCCCAGAT GGAGGAGGAG GACAGGGCCC CCCACAGCCC TCCAGAAAAG 780 GACACTGCCC CTCGTCCTTG CCACCTGCTC ATCACAGCAC CCAGAAATCT CTTCTCATGC 840 AAAGGAAGGC CAAGCGTCGA TTCCAGCAGG TGCCGCCTGT ACAGTTACCA TGGTGACCAA 900
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