Tag | Content |
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EnhancerAtlas ID | HS138-22040 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr2:173113100-173114370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr2:173114134-173114145 | AAGTAAACAAA | + | 6.62 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_36184 | chr2:173110932-173119589 | HMEC | SE_56556 | chr2:173110827-173119738 | u87 | SE_64808 | chr2:173111384-173119655 | NHEK |
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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 |
GH02I172246 | chr2 | 173111206 | 173120057 |
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Enhancer Sequence | TCCCAGAGCA CCCAGTCTCA CCCAGAACAC AGGTGAGCTT CCGGGTACAT CAGAGGTACA 60 TTTCCCACCC AGAAGGGATG CAAGTTCATT TTCACACAGG CCAAAAAGAA ACCCAGTTTT 120 ATCTGGTGGT GATTTATTCT TTCTCTCCCT AGCCACTTCT CTTGAGCCGA GTCTCCAGCC 180 TCTGTGGGTT TAATCTCTTA CTAATCCTCC ACCTCCCCTC CAGCATCTTT AGCTGACACT 240 CTTTCCTCCT GGCAGATGAT CACCACAGGC CTTTAAGGGA TGGTAAAATG AGCCAGGAAA 300 TAATCAGAGG CCCCAAGGCT GCTTTAGGTG ATGTTTGTTG GGTCTCACCC CCACTTCCTC 360 GGAGCTTCAG GTTTTCCATT CAAGCTCATG GATGCCACAC CCGGGGCATT CCAGCTGAGC 420 TCTTTGTAGC TAGCTGAGCC AGAGTTTGTA GACAGCTGGA GAAAAAAATG TGCTGAAGAA 480 GCAAGACCTC CATGCTGTCA TCCTGTTGGG ACTCACCCCA ATAGCCTCAG CCGGCTCTAG 540 CTTTAGTGGG TGCTGAGATG GTCTGCCCTG AGCAGTGAAA AATGTCAGGG GAGTGAGCAA 600 CAACAAAAGC CTGCATCCTT TCTCTCACTC CATCCTGGAG TTGAGAATGA CTGCAGAATG 660 AGCAACTATC CAGGATACAG GATATACTTG TCAAAGTGAG AAAGGTACCT ACAGGCCATT 720 TGGAATGACT CATGAGATTC CTACCTGATA AAGGAATGTC TCAGCCCTTC CTGGATATGT 780 ATTAGGGGAT GCTTAACTCT AGAAAACCCT CCTCAAATGC CACAGATGGC AAACTCCAGG 840 CTGTGTGTGT TTTCCAAGTA GGGAAAACCA AGGATATAGA AGGCGAGCTG CATTCTAAAA 900 TGATACTGAG ACACATGTTT TCAAGTGCAG ATTCTGGATT AAAATGGTAT TAAATGAAAT 960 AAGCAGGAGG CTATTGGCTT GAGGCTGAGT CTGTACTTTG AGTCTTTAAT TAACAAACTG 1020 CAACCTAGTT TAGTAAGTAA ACAAATTGGA AGTCTAATAG GAGCATAACA GTGGAGTCTC 1080 AGCCAATCAC AAGCAGCCAT GCTTTAGCCA ATCACAGGAA GCTGATTGAT CAGACCATGT 1140 CCAAACAAGA CAAATGCTGA GATGTAACCA ATAAAGCTCT TTCTGTCCTT TACTTCCTGT 1200 TCTGTTTATA AATACTGCCC ACACTGCAGA GTGAATTTCT CTGAATCTCT TCTAGTTAAG 1260 TGCTGCCCAA 1270
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