Tag | Content |
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EnhancerAtlas ID | HS179-16944 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr2:161171350-161172510 |
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) |
FOXP1 | MA0481.2 | chr2:161171560-161171572 | CAGTAAACAGAA | + | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_37535 | chr2:161171513-161172942 | HSMMtube | SE_44445 | chr2:161171011-161175445 | NHDF-Ad | SE_45573 | chr2:161171754-161175213 | Osteoblasts | SE_56333 | chr2:161171439-161175413 | u87 |
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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 |
GH02I160315 | chr2 | 161171726 | 161172650 |
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Enhancer Sequence | TCTTGGATGT TTTTTTAGAC ATCTGTTGTC CATGCTAACA CGCAACAAAG CTCTGTGGAT 60 ACACACACAG GCATGTACAT GCACAAACTC TCTCTCTCTC ATATAGTTTC AGCAGGTCAT 120 AAATGAGAAC CCAGCTACAA TGAAATGATA CAGCTTTTAC TGATGGATAT TTAAGTTTTT 180 TCCTTCAATT TTGCTATTGT CAACAAATTA CAGTAAACAG AAGATCTCAA TTTTGATGTT 240 ATTGTATTTG AAGTTACTAT CAACTCAGGT AATATTTGCA TTCTGTTATC TGTTATTTTC 300 TTATAGAGAA ATCCATAATG CCTGCATTTT AGTTAACTGT TTACATCCTT TTCTGGCCTT 360 TCCCAATGCC TACCACACTA TGGCTGTTTT ATAACCATTT GCTGAAGACA AACATAATAG 420 TTAAGTATGC AACCTTGTGC TCTTTCATGC TGTCTATCTG TATTACTTTC AAGTAAATAG 480 AAGACAATAT ACAATTTGAG TTATACAGAC TCTATGGATT TGATTATATA AATAGGTGTA 540 AAGACGTTTT TGAAGGCAGG GTTCACTAAA TAACATGGCA TCCTCTCACT GAGGCTTCCC 600 AGGAGAATTC CTCTCAGGTT TCAGGACCAG GAATAGTTAT GTTACTCCTG CTCTCCTCTC 660 ACATTGTGAT GACTGAATCA TGGGGCGAGC TATGTTTTCT ATTTTTGCCT TGGCCAGCAG 720 GAAACACAGG GACATTTGGT AATAACTTAA AGCTGCCTGC TTTTACCCTT ATTTTTCCTG 780 TTAGTCTAAT TCATCCTGAA ACTATTTTTG CTAATGTGTA TAAGTATTCT GGTCTTACAT 840 GCACTTCTGT AAGTATAAAT AATGAATCAA TCAATTTCAT AACCAATCTT TTGTGAGCTT 900 TTCTTTTTGT CCTGAACTGA CATATTTACC AGCATTGGAG GGCTTATAAA TGCCTTTTGT 960 TGGCTAAACT TTGAGAGAAA CTGAAATGTA AAATAGCAAC TGAATTGTGA ATTTTAAAAT 1020 TTAATAACTT AGGTACATGT TATTCTAATG TTTCCTTCAG CTTAATTCTC TTGAAAATAC 1080 ATGTTCCAAA AATATGTTTT GTGGCAAAAA ATGTTCTGTA ACCCTCTAAG ATCTCTCATT 1140 CCCATATATA AAGTCCTTTG 1160
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