Tag | Content |
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EnhancerAtlas ID | HS060-00626 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr1:26104820-26106100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr1:26105761-26105772 | TTCTTATCTGT | + | 6.14 | Gata1 | MA0035.3 | chr1:26105761-26105772 | TTCTTATCTGT | + | 6.62 | Stat4 | MA0518.1 | chr1:26105930-26105944 | TTTCCAGGAAGTCA | + | 6.13 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65420 | chr1:26104987-26105723 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH01I025776 | chr1 | 26103259 | 26104830 | GH01I025778 | chr1 | 26104988 | 26105723 |
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Enhancer Sequence | CCTGCAAGGG GAAGGGGCAG CAGGAGAGAC TGAGGCTAGA CACCAGGAAG AACTGGAAAG 60 ACCGGCAGCA GTGAGCGAAG GGAGCACATG GCCTTAGGGA AGCCTCCCCT TGGAAGTTAA 120 GTAGAATTTG AGAGAGGTAC TCTCCAGGCT CCGAGACCAT ACCCTGAATG AAAGGGAAAC 180 TAGTACAGAC ACAGGAAGCG CTTTGCATGT ACCTGGTACT CTTCCGCACT TGACACAACA 240 TCACTGAACC TCACCACACA GATGAGGAAA CTGAGGCTCA GAGATTACTT GGCCAAGGTC 300 CCTTGAGAGG GGCACAGAGT AAAGGATCCT CCAGCCCCGG AGGCAGAAAC GGCGGCTTCC 360 TGAGCCCGGC ACATGTCCCA CCCTGAGTCT CCTACTTTCA AATGTGCCTC TGCCTTTCCC 420 CCGGCACCCT CCTTAGAGGG GGTTTCACCG CCTCCTGCTC CCACCTGTTT AGTCGCCCTC 480 TTTGACCCAT GATCACCGGA AAGCCTGAGA GCTTGGTCCT CCCCACCCAC CACTCACCAC 540 TGAATTGTCC GATGCTAGAA TCAGAGGTCA CATTTGAGAG CCTGAGCCTG GCTCCTCATT 600 CTACACAGAG AAGTGGAGTC AGCCCAGAGA GGGGAAGTGA CTTAGCCAAA GTCACACTGC 660 ACATGAGGAA TTGATCCTGG GCTGGAACCC AGGCCTTCTG ATGCCTGGTT CCACCCCGTG 720 CGCAAACTGC ACCCCTCAGA AAAATCCCCA GCCCCCGTGT GGTCCCAGGA GACGCCCACC 780 GCTCTGAGTG GTAATCCCAG TGTTGGTTGG AGGGGACGAC CCAAGATTTG CAGTAAAAAT 840 CCCAGGCTCA AGCAGCGCTT GACAAAATGA CTGTTTTCTG ATGGCCAGGA GCCGCTACAC 900 CATTTGAAAA GATTAGAGAG GCCAGATGGG CAGCCTCTGT TTTCTTATCT GTTCGATGGG 960 AATCATGACA CAGGTCTCAG AGTGAGGCAC AGGGTCCCAT GAGAAAGTAC CTTGGCAGCC 1020 ACCTTTGGCC AGCAGCACTG CAGGCACTTG CTGACCGCCC ATCATGATGT GTCTGTGCCC 1080 GCCCCAGCTG AATGGGGTCT CCTGGAGCTG TTTCCAGGAA GTCAGAGATT CGCAATGGGT 1140 CTTTAAAACT GGTTGTCCAT TCTCTTCAAA GAGCTTGCTC TGCCAGGGCC ATAAACAAAT 1200 AAGAAATCTC AGGACTAATA AAAGGCTCGC TATTTGTCTG AGACAATCAG CCCAGACCAT 1260 AAAAGACAGC CGCTTAATAA 1280
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