Tag | Content |
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EnhancerAtlas ID | HS098-49058 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:82543310-82544680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr6:82543569-82543583 | TTTTATCTTATGTT | - | 6.14 | NR3C2 | MA0727.1 | chr6:82543756-82543773 | GAGAACAAATTGTTCTT | + | 6.08 |
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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 |
GH06I081833 | chr6 | 82543498 | 82544913 |
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Enhancer Sequence | CCTTCTTTTT GCAATTATAA TCATTGAATT TGGACTATGA ATCAAAGAAC CAGGTTCAAT 60 GCTGTATTTT TACCTGCATG CCTCTGACAT TCCATAGATT TCTTGGATAA TAATTACTCT 120 CCCTTTAACA ACACCATAAG TCCACTTAAT CTATGAATTT GAACCTTGAA CAAGAGATAA 180 CTGAAGAATT ATGTAAGAAA GAAACAGAAG AAGTGATGTT CTCAAGCTCT GGAGATTTTC 240 AGGCAGCTTT GAAAATCTTT TTTATCTTAT GTTTTATTCC CATAAAACTT AAAATCCTAC 300 TGGGGCATTA AGGTAGTAGC GGAGGGGTAG TTTTTCAAGA TGTTCTTGTA CAGCTTCCTT 360 CTAGAAATAT CTAGAGTTCT CCAAACTACG TTTGAAAACT CACTAATTTA AGACTTGTAA 420 CTTTGCAGAT GGACTTTCTT ACCTGGGAGA ACAAATTGTT CTTTTCTGCT TCAAGGAAAT 480 TTTAAAATGC TAAGTAAGGC TTGCTATCCT CAGAGGCAAC ATTGGCATCC TGAAACAATT 540 TTGGCCATCT GATTCCTGAG GGTTTGGCCA ACAGCTGTGC CCAAAATGGA TAATTGTGCC 600 TGGTTAAGTT TAGTCCTCTC TGACATCACA CATCACAGAG GAAATCAGCC CCACACATTT 660 TTCTTCAAGG AGAGAAGAGA ATTCATACAG ATGATTCAGA ATCAAGGAAT GAAAATGACA 720 ACAAGCATGC AAATGTCACA CTGAAAACAA AAATCCCTCC TAGTTCATTG GCTAAAGAGA 780 CAGTAGAAAC ATCCTGGGTG GAACTGAGAG CTGTGACTCT TGTGCTCGGT GGCCTGGAGC 840 CATTCACAGC ACCATCGGGA AGTGAAGGCA GGGAGCAGTG CAAGGCCCGT TGTGTCTGTT 900 TACCGAGTTC TGTAGGCCTT ACCAACTATC ATGTAGTAGT CTTTTTATGG AAACTAGATA 960 AACAACATGC GTCACCATGG CTATTTCCCT TTATCAGAGA AGTGGAAGAA AGACTTCTAC 1020 AAACTGTAGA TATCATGGAA GTGTGTGGGC CTTTCCAAGC TATTATTGCA CAAAATCAGA 1080 AAGAAATTGA AATGTTTTCT GCCAACGACT GATTATTTTT ATCCAAGTCA GACAGAAAAA 1140 TATTTCTAAA CATATAGATG TTTACCAGCT GTTCCCAGAG GCATTCATGT GACTGCAACA 1200 TCCTTTCTAT CAGCCCTTTA GGTTTGGAGT TTTCCATGCC AAAGAGACTG AACATCTTCT 1260 GCATTTTAAC CCCAGCTCAG AGACACTTCC AGGAATTCCA GTCCTCCAAG ATTTCAATGT 1320 CTTTATTCCT GTTCTACACT TCAGTTTTGT GCTGAAAGCA TCTAAAGGAA 1370
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