Tag | Content |
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EnhancerAtlas ID | HS129-06302 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr11:27444380-27445830 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr11:27445170-27445184 | ATTCCCTTGGGAAT | + | 7.47 | EBF1 | MA0154.3 | chr11:27445170-27445184 | ATTCCCTTGGGAAT | - | 8.42 | Sox3 | MA0514.1 | chr11:27444639-27444649 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64917 | chr11:27442229-27445729 | 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 |
GH11I027419 | chr11 | 27441472 | 27446226 |
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Enhancer Sequence | AACAGTATGA GAGAATGCCA CTGAGATCCC ATGGGGTATT TACAAGAATT TCTTACACTT 60 CTATTTTCAA CTGTTTCTAT AGAACTGGTG ATAAACTGAG TTAGCTGTAT TTTCACTCTG 120 CTACTCCTGG GTTCTATTGA GTTTTTAGAA GTATACATTA ACATCGTGAC ATTTTTTTCA 180 CTTACTGTGC ATAAAATGTT TATACATAAC CTGATAAAAC CATCCCTAGA TAACATATTG 240 ATTTTAAGAT TAAAAAAACA AAACAAAGGG AAAAAAACAC AAAAAACCTA CACTCCAGTA 300 AATCCCTCCT AATGCCCCCA GTCTGAAAGG GGCCTTCCAA TAAGCACTGT TTGTACATCC 360 AATAAGTGAC CTAGGCAAGA ACAGCTCCAG TTTCTAAGAC ACTAAGGCAC TGACCTCATT 420 ATGTTGAGGC AAGAGGAGAA TTCTAAATGA TGAGGCAATC CATATACCCT GAAGACCAGC 480 TGCCAACCGT CAGAGCCTGA ACCCAAAGGC AAGCTTCCTG GGATTTCACC ATCCCCATAA 540 TGCAGGCTTG TGGAGCAATC ACTTCGCCTC AGGCGATGAG GCGTGCAGAC TCCCCTCCCA 600 AACACATACC CCACACACAC TCTCTCTCCT TCTCCCCTCT GCTCTGATGG CCATTTTTTA 660 AAGGCTTATA AAAATGTATT CTATCCTTAA AGAAATGACT CAAAATTATA ACTGGGATGA 720 TTCAATTGTT TCTATTAACT GTAAGACAAT AGACATTGAT AATGATGGTT TATAAAATGT 780 CACTAGAAAT ATTCCCTTGG GAATGACTTA TAACTCATTA AAATCACTAA TGATTTATTC 840 AGCAGAGAAG AGGCTATGCC ATCAGAGCAT GACAATGTCC TGAATCTTGG GGAGCAAATA 900 TTCTTAAACC TGGTTTGTAA TACTCTTGGA CAGCTCCACT TGTGACAAGT CTTTAAGTTC 960 TAAAAAGTCC CAGAAACAAA CAAAAAGGTT AAATTCTTTT TAATTTTTGC AATCAGAATG 1020 AATCATATGG TCCCTTGTTT CTTTCTCCAG GGAGAAAACA ACGTGCTACC ATGAAATTTG 1080 CTTAATAAGA AAAAACAGAG AAAAAGCATA CACACACCCA GACACAAACA TAAATTTCAC 1140 GGCAGAACAT AGTTTTCTGT CCAGAGAAAG ATGACTGAGA GTTACTGCTT TATGACATTT 1200 ACCTGAGAAA ATTTCTCAAT TCTGCAGTTG ATCTGGTGTT TTATTGAAGC AGTTTCTGTT 1260 ACTAAATTAG TAAGCAGAGA AACAAATGTC TTAGAAAATA AGCTCCTACA AGGAAGAGAA 1320 TATCTAATTC CTCTAACCTC CAGCAAAACC AGCCACACAC CTCTAATTCA CTTACATACA 1380 CACACACATA CACATTATAA AGACCATAAT CTTAAAGAAT ATAAGGCCAA GCACAGTGGC 1440 TCACCCCTGC 1450
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