Tag | Content |
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EnhancerAtlas ID | HS007-13955 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr5:158657240-158658640 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Twist2 | MA0633.1 | chr5:158657724-158657734 | ACCATATGTT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_36658 | chr5:158657391-158658463 | HMEC |
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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 |
GH05I159230 | chr5 | 158657392 | 158658463 |
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Enhancer Sequence | ATTTAAACAG ATGCAAACAG CGAGCACATC TTGTCACCTT TGCGGGACTG TGGCTGTGCC 60 CCTCGCAGTA AATTTGGAGG TTCTACATCC CTGGTGAAAA ACAAAACAAA ACAAAAAAAA 120 AGCCTGCCAT CATTGACACC AAAACACTCA TAATGACAGT ACCCACTGTA ATGCTTAGAA 180 GTGAAAAAAT AACATGCCAT GAAAGAGACT AATTGAAGGG GCTTAATTTA GATCAGGGGT 240 TCAAAGATCT CTCTGGAAAG TGCCTTGTGA GCAGAGACTT CAGAAAGAAA GTTTAACCAA 300 AGGAAAATCA AAAAGAAGAG TGGTCCAGGT GGGATCCTAG AGAGAGCTTA GTATGACAGA 360 GGAATTGAAG GAAGTTGGGA AGTTCAGAGA AGCTGGAACC AAGTAAGTCA GAGGGAGAGT 420 GGCATGGATG GGACAGGAGA GGAAGCTGCA GTCAGATCAT GCAGGCCTTT GGAGACCGGG 480 TTAAACCATA TGTTATATAA ACACAAATAT ACAAATCCCT AAATGTAATG GAAAACCTCT 540 GAGGATTTTA AGCAGAGGTC GGGGTGCTGA GTATGGTTGA ATAGCCTGCG TACTGCACAA 600 CTCCATGTTG CACCAGTGGC ATAGTTCCTG GTGTGATGCA ATATTGCCTC TGGGCAGGTA 660 ACACAATCAA ATTAGTGTTA AACAATTACT CTGGTTGCTG TAGGGAGAAG AACTGTAGAG 720 GTAAGAGTGG AACCAAGGAG ATCATTTAAC TAGCTAATGC AGACTCCAAT CAAGTAGCCT 780 AACACAGTAT TTGTGGTGAT AGGGAAAAGT GGACAGACTG TTTTTTTTTT TCTATTTCCA 840 TGGCAGACAG TAGAAGTCTG GGTAGATTTC TGAATCTGAA AATAACCTAT CTTAAATGGT 900 GCTTGAGAAA AATTAATCGT CCATCCAGAA ATGTGCTAGA GCTGATATAC AGCAGCTTGT 960 ATTGGTTCAG TAGAGACAAT GGGGTCCACC TTTCCCCAAC TCCTCATTCA GTGACATCAA 1020 GTTGATAGCT TGAAATCTGC CTTGGTGGGA GTATTTATAC CATGGAGATT AGCAAACACT 1080 ACCAATAGAG CTTCTTTCCC CAGAGAGCTG ATTGTGAAAC ATTTACCAGC ACACCAGTGC 1140 TTCCAGTGCT TTTCGCTATC TCAACACTGG AATACTATTT AAAGAATCAC TGCATATAAT 1200 ATGATATGAT GTCAAAGAAC ATTCATATGG TTCTTACGAA ACCTTAAGAA AGGAATGGTT 1260 ATGAGAGACA CTGGGAAGAA AATATCTGTA AGACTGGGTG GTGCTTTGCA AATGGTGGTA 1320 ATGGGAAGAG GGGGAGCAGA TTGTATCTTC TTCCATGGAA TAGGAATCAT TTCAAAGCAT 1380 ATATCTTTGA TGAAGATTAC 1400
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