Tag | Content |
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EnhancerAtlas ID | HS177-24150 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr9:128408900-128410060 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr9:128409021-128409042 | GAAGAGAAAATGAAAGTCAGC | - | 7.17 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09553 | chr9:128407516-128416412 | CD14 | SE_32603 | chr9:128407122-128415730 | GM12878 | SE_38321 | chr9:128407951-128413819 | HUVEC | SE_46547 | chr9:128406690-128414609 | Osteoblasts | SE_56438 | chr9:128409074-128413753 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 128409698 | 128409918 | chr9 | 128409576 | 128409671 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I125643 | chr9 | 128406147 | 128414810 |
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Enhancer Sequence | ATAACATCAT TTAAAAAGAC TTGTTTTAAA GCTAGAAACC TAATAAAATA GAAAGAGGAA 60 AAAAAGGTCA TCATGGTTGA AAAAAGAACC CAGCAAGTTA TTGTTTTGAT ACCATAATTA 120 GGAAGAGAAA ATGAAAGTCA GCAAAACCAC AGTTTTAGAA AAGTGGTTAT TAGATTTTCT 180 TCTTTCCACA GTGGAAAAAG TCCTTCCTGT TGAAGAAGGC AGTGAAATTT TATCACAGCT 240 ATTGCTATTC ATAAATCTTA TATCTATTTT AATTCAATCT GGCCCTAGCC TCAGAGTCGC 300 TGCACCACAA TTTGATTACT ATAACCATAC TTTTTAACTG CTGTCAGGAA AGACAGCGCC 360 TTATACAAAC ATCTGCCGGA ACACATGCCT GCGTTCTCCA GCACCAGCCT TAAATCACGC 420 TCTGGTGATG AATCTTTATC TGACACTAAT ACTTTTTAAC TTCATACGGA CAATTAAAAT 480 GAATTGTAGC TAAATGCACA TATAACAAAT CAATTTAATC TTTGGTTGCA TAGCAGCATA 540 TTTTGCAAAT TTCCTAAACT TACATGTATT TTGTAAAATT TCTTACATGT ATCTTTGTCT 600 AGGTGTTAAA CTTCAGTTTA ACAGAAAGTA AAGTGGAAAT ACTAATAAAA CACAGCTCTT 660 ATGATACTGC CATGTAGTTG CAAGCCTCAA AGAATAATGA CATTTGAAAT TTATCACTGC 720 CATTTTTAAA AACTTCCACA TTTCTATGTG GAGAGTACCA TTCTGGGCTT CATTATAAGA 780 GTGACCAAAG CTGAATTCCC TGGCCTGTAG GAATACAACT GAAATTCGGA CAACCACACC 840 AAGGATAAGA AACTGGCTCA GATCCGAGCC GTAGACAGTA TTCATCTACT ATTCATCTAT 900 AGTGCCCATC ACATTTGCTC TCTGGTTTGT TGTTCGTGGT TCTGTTCCTC TGCTCGGTCA 960 GGTGCACCTA ATGTCATGGA CCACTGTCAC AGTCCTCAGC ACTGGGCACG ATCATTCATG 1020 TAAAGTATAG TTTCTCCACT TGATGGCCAT ATGGCCGCTC TTGTCTTTTA AGTTCCCCAA 1080 GGGCAGTCAG CCCCATTTTA TTTATCAGTG CACGGTGCAG AGCTGGTATG CAATAAATGT 1140 TTGAAATGAG CCAGTACAGT 1160
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