Tag | Content |
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EnhancerAtlas ID | HS082-19687 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr2:172203520-172204900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr2:172204715-172204729 | TTTCCCTGGGGAGT | - | 6.06 | JUN | MA0488.1 | chr2:172204399-172204412 | AGAATGATGTCAT | + | 6.78 | JUND(var.2) | MA0492.1 | chr2:172204398-172204413 | TAGAATGATGTCATT | + | 6.6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_32499 | chr2:172202207-172205404 | GM12878 | SE_60987 | chr2:172170904-172218541 | HBL1 |
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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 |
GH02I171346 | chr2 | 172202840 | 172205192 |
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Enhancer Sequence | GCTTACGTGT GATAAGATGG TCACCCCCAT AATGTGTTCC TTCTCCCTGC AGTGGTCCCC 60 TGACAGGTAT AAAGCCCATC ACACTGAAGT GTTACAGAGG GGATGCAGAA GGGACCTAGC 120 AGAAGCCTTT ATCTCTTTGA GTCATTTTGA AATGGAATTT TTTGTTCTGT GTCTCTGCAG 180 CAGTCAGAAA ACTTGCACAG AAAGAGACTG GACATACTAA TAAGCAAATC AAATGCTTCA 240 AAGTGGTATC ATCAACCCTC TCCTGCCTGC CTTTCCTGCT TCTACAGAGA GAGGCCAGTC 300 ACCACCTTTC TATTTCAGTC ACACTACGTA CGGTTCTATG GGAACTGTCA TTTTCCTTTA 360 CTGCGGTTTC CAAGGCCCTA AAATAACCTT CTCATTAGCT TCACCAAGTT CATTGTTAAC 420 ATAAATAGGA CAAAATAGGC AGCCACATAC AAACGACTTT AAGGGAACAC TATCAGCACT 480 GCTCATCTAT TTATGTTCTA AATGGAAATA TTCAAAATAG GGCAAAAAAA TCCTTGGTTT 540 TTCATATTAT CAGGAAATAT ATTGTGGATA ATTTTTAACT TCCTGGAAAT GAATTAAGAT 600 GGCTGACAAC TTTTAATTCA GTTTAGGCTT GACTCTGTCT GTCACATCCA GGTGGCCACC 660 AGCAGAAGCT TGAGTAATGT GGAAAATATG TCTGTGCAGC TGCTGGCAAA GAAGCACAGT 720 TATACTTCTT CAGAAACAGT GTGACAGAGT TCCTGCAAAG GAATGCAATA TTGGCTGATT 780 TGTAAGCAGT ACTGCCACTG GTATGCACCC TCGAATCCAA CCCTAATACT CTCTGGCCAT 840 ATTCCCCTCA AAGACTTCGT GGTTGAAGCT CATAAAAATA GAATGATGTC ATTGTGGATC 900 AGGTGCTCTT CATTTCTGTC CACTCTCCAG GATACAATAA GGAGCTTAGG AGGAGGATGG 960 AGAACTGGCT CTACGGAATA GCAAGTGATA CCAGAAGATA AGATAGGTAG GCACTGCCCT 1020 CTTCACTAGG TAAGGGCAGC TAATGAGGGC AGTCTCATTA GCTTAGGCTC CCCAACTACT 1080 GTTGCTTCAA ACTTTGGCCT CAATTTGTAG ACTAAAGTCA CCAGAACAAT AGTTAACTAC 1140 CAGTGGGATT AGTGATCTTC CTTATACTTG GTTTACACAG AGGAATGCTA ACATCTTTCC 1200 CTGGGGAGTT CCAGGACAGC TGATCAATCT AGAAACAAAA TTCAATCTCA GGGGTTGGAA 1260 ACCTTTTTCT GTAATGGGCC AGATAGTATT TTAGTCTCTG TGGGCCAGCT GCAGCAGTCT 1320 TTGTTGCAAC TACTCAACAC TGTGACTATA GCTCAAAAGT GACCATAGAC AGTATGTCAA 1380
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