| Tag | Content |
|---|
EnhancerAtlas ID | HS174-04991 | Organism | Homo sapiens | Tissue/cell | SK-MEL-5 | Coordinate | chr5:43622740-43624130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:43623047-43623068 | TCTTTCTTTCTTTTTTTCTTT | + | 6.34 | | IRF1 | MA0050.2 | chr5:43623037-43623058 | ATTTACTTTTTCTTTCTTTCT | + | 6.48 | | MEF2A | MA0052.3 | chr5:43623881-43623893 | GCTATTTTTAGT | - | 6.18 | | MEF2B | MA0660.1 | chr5:43623881-43623893 | GCTATTTTTAGT | - | 6.62 | | TFAP4 | MA0691.1 | chr5:43623614-43623624 | ATCAGCTGTT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAATATAACA ACAGTCTGAG AAGGCACTTT GATTGCTGTA TTGCAGATGA TAAGCAGCTT 60
GCCGAAGATC ACCCAGAACT AGTTAGTAAC AGAGTCAGGA TTTTGACCTA AGCTCTCTGA 120
CTCTTACTCA CTGTGTCTTT TTCTTTACTC CATGCTTTAG AGAGAAAAAG TAAATTTCGA 180
TAGTAAGATC TGCTGCTTTT GTGCGATTCT GCTTTTTTAA ATTATGGTTT TTTTTTTTTT 240
TTGTTATGTC TTGATTCAGG ATAACTTGGC CAAGTCCTGT GACTTTTACT TATTTTTATT 300
TACTTTTTCT TTCTTTCTTT TTTTCTTTCT TTAAGTGGTG ATGGAGCTTC TGTGTGGAAG 360
AGTTTGGTGC TTTGAAGCCT AGAGCCTGCT TATTCCCTCT GGTCACTCTT TGCCCCATTT 420
CCTATAGACT TACCCCTGTC CCCAAACACA GCACCAAACA CCCCATTATC AAGATCAATT 480
CACATGACCT CTGAGACACT GCCCAGAGCT CACTGGAGCA CAGTCTGACT AGCCTAGTCT 540
TTGTAAAGGC AGAAGGACAT GTGGGCATGA TGGGTGGGTG GCAATTTGTA AGCTTCACTG 600
ATTCTGTGGG TGGCATTTTT TTTCTACAGG AACAAAGTGT TGCTTTCAAT TGACTGTTTA 660
TGGGATATAT AACAGGACTT TACTCTGGAA GGCCCGTTCC AGACTGGAGA CAATGTTCTT 720
ACTTTGTTTC TTAGAAGGCG GGGGTAGGGG GAGACTTGTT TCTGAGGAAT TTTTTGGTTC 780
TCTTGTTGCT GATCCTTCCA TGATTAGGGA CATTAGTTAC ATTGCTTCAG ACTTACGGAG 840
AGTTGCTCAA AATGGTTCAG AATTGTGGTT GCTCATCAGC TGTTCCTTTC AGAAGCATTT 900
TGGCTGAAAA TAGAGGTTGG GGTAGATGTT TCACCAATGT TGTACCCATC TTTGAAATGT 960
GTTTTGATGT TTGATGAACA AAGAAAAACC TTATAATTTG ATAGGGTAAA GGTAGTTAGA 1020
ATGCCACACT GGGACTTTTA GTAGAAGGAA CTTTTAGACA GTGGAAAAGA ATCTGTTAAT 1080
CTTCAACATA CGTAATGCTG ATCATGCTTA GGTAGTTTTA CACGGATATT CTGATTATTA 1140
GGCTATTTTT AGTGAATTGT TGTTGGCCTT TGCTAGCAGT TGTTTCTTTG ATAAAATTTC 1200
AAGATCAGTG GTGGTTCAGT TAAAGAATAG TCTATGTACT CCATACAGTT ACTAAGGGCT 1260
GATCATCATT ATCACCATCT GCACCGCCAT TTATTGATGC TAAACTTATA CTAGGCACCA 1320
ATAATTGTTA GCTGATGATT TTTCATTATT AGTTGATAAT GAGCCTTAAC ACATAACTGG 1380
GTCTGTCTTC 1390
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