Tag | Content |
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EnhancerAtlas ID | HS142-03122 |
Organism | Homo sapiens |
Tissue/cell | NCCIT |
Coordinate | chr2:16120260-16121200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr2:16120585-16120596 | ACAGGGTGTGG | - | 6.14 | MEF2C | MA0497.1 | chr2:16120427-16120442 | TTCTATTTTTATCCT | - | 6.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 16120365 | 16120600 | chr2 | 16120600 | 16121000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I015979 | chr2 | 16119952 | 16121482 |
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Enhancer Sequence | TTTGCTCATA TCCTCATCTC ACAGACACTG TGTATCTACT TACACCATTC ATTAAATAAC 60 AGTAACAACA ACAAATACCT CAAGCACTTA TTATGTGCCC CACACTGTCT TAAGTGCTTT 120 ATGGATCTTA ATTCATTCAT CACAATGACC CTAGGAGGGG CCTATTGTTC TATTTTTATC 180 CTTATTTTAC AGAAGAAGAA ACCAGAGCAC AGAGAGGTTA AGTCTTTCAC TAAAAGTCAC 240 ACAGCTAGTA GACTTTGGGG CCAGGATTCA AATACAGGCA AACCACAGGT CTTGACCCCT 300 ATGCATGTGG CTTGCCCTGA TCACCACAGG GTGTGGGATG CCTTTATCCG CTAGCACTTT 360 CAAAGGTCAT TTTCAAATGG CCTTTAGCAC TTTCTGCCTT GTATGAAGCC TCGGTATCTG 420 GGATTTCACC TTCTCGGGGT CAACCATTCC AAAGCCCCAC TGGAAGTCCC AGCCCTGTGG 480 ACGTGGTATT TGGTGGCGAT AGCCGATCTG AATTGTGAGC CGGCCCAGCC CAGCGCAACA 540 TTTGCATCTC AAAGAAGCTC TGTGATTTTC TCGAGATTCC AAACACAGTA ACTGCGGGGA 600 GGGCCCCATG GTATTTGCAA GGTTGAGAGT TTGCAAATGC CTGGAGGCTG ACCCCTGGAT 660 CTCCTTCACC CCGGAGACCG ACCAGCACAC CATCTAACTC AGTGCCTTTC ACATCGTATT 720 CAGTCTGAGA AACAGTTTTG GTGTTTTGTT TTTTCCTACC GTGTGCAAGA CAACAGATGT 780 TTGGTGACTG CATGAAAGAA AAATTTTTTT CTTTTCTTTC ATTTTATTTA TTTATTTATT 840 ATTGTTATTA TTTGAGACAG AGTCTTGCTC TGTTGCCCAG GCTGGAGCGC AGTGGCACGA 900 ACTCGGCTCA CAGTAACCTC TGCCTCCCAG GTTCAAGTGA 940
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