Tag | Content |
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EnhancerAtlas ID | HS095-17679 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:225306780-225308050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr2:225307302-225307314 | CACCCCCTGACA | - | 6.22 | NFKB1 | MA0105.4 | chr2:225307158-225307171 | GGGGGAATCCCCG | - | 6.36 | NFKB1 | MA0105.4 | chr2:225307158-225307171 | GGGGGAATCCCCG | + | 6.46 | ZNF263 | MA0528.1 | chr2:225307477-225307498 | GGAGGAGGGGAGCGCGAAGGA | + | 6.23 |
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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 |
GH02I224442 | chr2 | 225306718 | 225307917 |
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Enhancer Sequence | TTTGAGCTCA AGGGACATGG ATTTGGGAGG AATTCAAAAT GTGAAGCCTA ACTCAGGATT 60 CAGGAACCAG ACTAACAGAG GGCAATGAAA CAAAACCAGA GAACTCAGGC CCAGAGCCAG 120 CGAGGGAGAG GAAGGACGCC GAAGCGTAGC GTCCCGCGCC GCCCCCCGCC AACCCGGGAG 180 GACGCAGACC CCCCAGAGCC GGTGTCCAGC CCCACCTCTC CGGGCGCCTG CAGGAGGGGA 240 ACCGCGCGTC CCATCGCCCG GACCCCGGGC CGGCGGCGCG GCCGAGTCCC GCTGCTTCCG 300 CACTCGCCCC GGGACCCGGA CCCCCGCCCC ACCGCGCCCC TCCACCTCCC CGCCGGCCGG 360 TGCCACGTGT AACGCCGCGG GGGAATCCCC GGGGACACAG GGCTGGCTGG ATTCGCCTCT 420 CGGCCACAGC TCTGCGCTCC ACGAGCTGCT CCTGCCCGGT CCCCGCAGGA CTCGAACCCG 480 CGACACCTCT GCCGCGCCCT AGCCCTCGCG CCCCGCCGGA GTCACCCCCT GACACTGCCA 540 GGATCCCCGC CCGGCTGCGG GCACCACGTC CCCCGGGCCT TCGCGGGGCC CCGAGGGCCA 600 AGACCGAGGA CGCGCCGAGC CGAGGCTGCC TGGGGACCTG GTCCATCCGG TTCTGATGGG 660 GTCCGCAGGG AAAAGGCACT ATCCCGGAAA GCTTCCTGGA GGAGGGGAGC GCGAAGGACG 720 AAACTGGGCC TCCCTCTAGG CGGAGCTTAG TGTTTAAAGC TGGCCGGCCT TTCTCCTTTT 780 CATAGTAATT ATTCTCTCAC TAAGCTCAGG AAGCACGCCC TCCACCATCT CATTAAGCGA 840 ACCGGCTGTG GCTGACTCTT CCCTCCTCTA ACAACTGTGG CTCCTCATAG CCGGCACAAT 900 GACGTCCAAA GCTGTCGGCT CCCGCACGGG TTCCTCCCTT TGAGGCTTGT CTTTCGCACT 960 CCTTCCACCT GCTCGGAGAA CTGCGCCCAG GTGGGTTCAG CAACTAGCAG GTGCCATGAA 1020 GAGACCCTCA GAGAAGCGGC CGGCCTACCT GGCGCCCGTT ACCCCTCTCG CCGCAAACCC 1080 ACTTCCCTGA ACTGTTTTGC AGTTCACAGC CTCTCTCCCC GCTCTAAAAA CTAAAAACAA 1140 ATGAACACTG AAGAGCTCCA GGCTTCATTT TTTTTTTTGA GACGGAGTCT GGCTCTGTCG 1200 CCCAGGCTGG AGTGCAGTGG CGCGATCTCG GCTCACTGCA AGCTCCGTCT CCCGGGTTCA 1260 CGCCATTTTC 1270
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