Tag | Content |
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EnhancerAtlas ID | HS098-40176 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:138127120-138128510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFK | MA0496.2 | chr3:138127650-138127669 | ACCTGCTGAGTCAGGATCT | + | 6.17 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_37071 | chr3:138126193-138133527 | HSMMtube |
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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 |
GH03I138408 | chr3 | 138126956 | 138128620 |
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Enhancer Sequence | GGCTGTGCCA CTGAACACTT AGTAATGGGC TGATGTTTAT TAGCCACACA AAAAAAAGGA 60 TGGTCAAACA TGTCCATTCA TTCAGGCAGC ACACACTCAC TGAGCTCTGA GCCCCACATC 120 AGGGCTGCAG AGAGCATTAA AACCTGTGCA GCACAGGGTT CCCAGCCTCA TGGGGATGAT 180 GAGCTCTGGG GATCTGTGCA TTAAGAGGAA TGCTCTGACC TGGAGGAGCT CCCATAAATC 240 TCAGTCCCTC ATAATCCTTG TACTCAGTAG ATGAAGAGGG TGTTCACTGA CCAGATGAAG 300 ATTTTAGTCA CATTTTGGGC CCACTACTTC CATCACTTTT GAAGATTGAA GGTTTCCCTT 360 TCTAAAGGAT GCTCAGATTC CCAGGTCCAT ACCAGGACTA TTTTAAAGTC CACTTTCATC 420 TCCGCACACT TCTAAAGAGG CTGTGAACCG AAGTTCCCAG GTGTCACAGA CGTCAGCATT 480 GTCATCACCC AGGAGCTTTC TGGAAAGGCA GACTCCTGGG CCCTGTCCCA ACCTGCTGAG 540 TCAGGATCTG CATCTTAACA AGATCCCAGG AGAGTTGTGT GCACAATGAA GACAGTAGCC 600 ACTGCTCCAG AACATCAGGC CTGGCATCGA AATGAAATCC AGCCCTGGAC TCACTGTTCC 660 TCAGGATCCG GTTCAGCTTC ATCCAACCAG AGGATGCTTC ATCTGCATTC ATTCGATGAC 720 TAAAAAGTTC GCGCCTCTGC CTTTAACAGC TGCAAGATTC TGCCCAGCAA GGAGGAGGCA 780 GTGAGCTCCA AGTGCCCACC CACGGTCAGC ATGTGCTTCC CTTAATTATG GGAAGTTTTC 840 ACACAGAGGC AAGTGGGCTC CCAGTTTGCT TCTCAAACAC TTGCATTTTG GTTAAAATGC 900 ACAACTATTG TAAATGTAAA GAACAAGAAA AAATCTAACT GCTGAGAACT CTTAGGGACT 960 CCCAGTCCCT AAGCACTTGA AAGGGTGGCC TATTCTGTGC AAGCTGGATT TTCACTTAGC 1020 ATAGCTGCTG GGCTTCCACA TCATCCTAAA TAGCTCATTA CCATGCTAAT GTGGAAATTT 1080 AAATATAAAA AAGGAAAGCT GAGTTTATAC CAAGCAAAGA ACTGATGGAT GCTTTCAGTG 1140 GAATGTACAT CCTGGCAATT ATGTGCTAAA CCATTAGCTC TGACTCAAAT CCAGCTTCCT 1200 AGTCTCTCAT CAGCCCTCCG CCTGGGCTAA TGAGCAGAGG TGAAATCACT GGATAAGTGG 1260 CTCTCAAAGT GTGGCCCTCA GACCAGCAGC TTCCATATCC GGGGAGTCTG CTAGAAATGC 1320 AGGTTATCTG GTCCCACCCC AGACCTAATG AATCAGAAAT TCTGAGGTGA GGCACAGCAA 1380 TCTGTGTTGA 1390
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