| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01547 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr1:44792520-44794850 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:44793382-44793397 | AAGGTCCAGAGTCCA | + | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I044325 | chr1 | 44791531 | 44795579 |
| Enhancer Sequence | CTTTATTTGA GGAGAGTATG GGTGCAAAGT GAATTATAAT TTACCCTTAT TGAAATCTGA 60
ATTTTTCAAA AACATAATAC CAATAAATGA AGGAGACCAA GTCTTAGAAA CCACATCCTC 120
ACCTGAGGTG TGCACACCTG TGTCTCCCTC TGTATGTACA TGACTCAGAA ACAGCCACAG 180
TTCAAACATT TTTACATATT CAATTGTAAA TAACTTCAGA TATTAGTGGC TTCTGTGAAG 240
CTGACCCTTC AAGGGCACCA AACAACCAAA TGATTTGTTT GTAGCTACCT GTAGACACAC 300
ATTTGTCATG AAATTAATTT AAACAAATCT CAGGTTATGT GCTAGAGAGG TCCCCTGGAG 360
GCATCACTAA GGAAGGGCCT AGAAATGGAA GGGTGCCAAG CCCAAAAAAA TCTCTCTGGA 420
TAGTACTCTG GTTCTATCAG TATGTTGATA AGAGGGCCTG ATCTCTCTGT GTTTCCCAGA 480
GAAGCAGGGC CTGCCTCCCA GTCACCTGCT GTATCTCAAC AGCTTATTAG GAGGTTGTGG 540
ATCAGAATAA TACTAGTACT AGTTCTACTA ATAAGAGCTA ATACCTATAA GCCATTACAT 600
ATCAAACACT GTTTTGAGCA CTTAATATGT TTAACTCAGT TTATCCTCCC ATCAGTCCTA 660
TAAGATTGGT ACTATTATTA ACCCCACTTT GCCAATAAGG CAACTGAGGC ATAAAGAGTG 720
CAAGCAACTT GCCCAAGGTC AGACTACCAG TAGGTAGTCA AGACTCAAAT CCAGACAGTC 780
CAGTTTTGGA ATCTATGCTT TTAACTACTA TGCTCTACTG ATTCTCATCA GAACAGCGTC 840
TACCTCAGCT TCCCTCACTT TGAAGGTCCA GAGTCCACAT TCTGGGACTT GGGCACATGC 900
AGCCAAAGCC TGTTCCATCA GTCACCCAAC AAAGTGGAGG AAAGGCATGT GTCTTGCTCA 960
GGATCACAAG ATGAATCAGA GGCTTGGTTA GACAAAGACC ATTTTTCAAA CCAATTCAAA 1020
TATTGCCTTA AGATACACTA GCTGGGGGTG AAGAAATGGC GGTGAGTAAC AAGTGATCAA 1080
GACAGGACCA GGCCCACTCA GGCAGACTGA GAATTCTGGT CAGACTACTT GGCCAGGAGC 1140
CAGGGAAGCT GGCTGGGCTA CAGGAGGCCT TGCTCAATAA TCCCCATCCA TAGCCCCAGG 1200
GACTGCTGAT CTCTTCACAG AATACTGCAT GCCTGTGGGG TGGTTCATAG ATTCCCTGTT 1260
CTCTGCCCAC AAATGATGGC CAGCAGCCAG GAAGGTAAAC AGTTGTGCTG GCATGACAAT 1320
AGATTTTTAA AAATTCACTG ACTAGTAAGC AAGCAATACA CAAACGGATA CCCGCCCCCC 1380
ACCCCCGCAA TGCACTGAAC ACATTTCTCA CACACTGTCC CATATGATCC CACATCTCCG 1440
TAAGCAGGCA GGAATCACTC CCCTGTTTTG CAGATGAGAA AGCTAAGAGG GTCAGCTGTT 1500
GTCAAACCAG TCCCATCACT TGAGAACTTG TTAGAAATGC AAATTTCTGG CCTCCACCCT 1560
TGCCTTTCAG AATCAGAAGC CCTGGGGATG GGGCCAACAG CCTTGGTTTT AACAGCCCTC 1620
CAGGTGACTC TGACGCTCGC TGAAGTCTGA AGTTTGAGAA CCGCTGGTCC AGACTACAGC 1680
AGTGTTTCTC AGACTTCAAA TGACCTGAGG AATGTGTCAG ATTGCAGGTT CTATTTCAGT 1740
ATATTTAGTA TATTCAGATT ATATTTCAGT ATATTCTATT TCAGTAGGGC CGGCATGACA 1800
TTCTGCATTT CTAACAAGCT CCCAGGTGAT GAGGATGCTG CTGGTTCTCA GACCACAATT 1860
TAAACAGCAA AGGTGTAGTC TAGAACATTT ATGTGACTAA CTCCTTATCG CTGAGGTACT 1920
GACCAAATGA GAATCAGAGC CCATGGCTCT CAGCTCCCTT CTCAGAGCAA ACCCTTACTT 1980
GACCCACTTT AAGCACCCGA GTCAAGCCCT CTAAGTCTGC TAACCATCGC TAGCTCTTAT 2040
CACCAGACAT TTCATCCTCC TTGCTGCCAA GAGCTAGGGC AGAAAAACAG GCCTGTCACA 2100
TCCAAGAACT TCACAGAGTA GACTGGCACA TCTCTGTCAG GGAGCTAGCA AAAAGTCTTC 2160
TTGTCATGGC AGTGCCTGCT TCCTTTAGGA ATACTGTCAA GACCAGGGCA TCAGCTACCC 2220
TCAGAGTGCT CAGCACACTA TTGTCTCAGC CCTCCAGAAA AAAACCTTCC TCTGTCCAGA 2280
TGAACCAAAA AGCAGGACTG GGTACCTCTC CTATGAGAAG ACCGCTCATT 2330
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