| Tag | Content |
|---|
EnhancerAtlas ID | HS133-04286 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:29264130-29265690 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr10:29265176-29265187 | TTCTGTGGTTT | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr10 | 29264721 | 29265324 | | chr10 | 29264901 | 29265000 | | chr10 | 29265000 | 29265201 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I028975 | chr10 | 29264534 | 29265583 |
|
Enhancer Sequence | GAAATGAGAA AGTGCTGATC TATACTTAAA TGGGGGCTGG GGTCTCACCT GCTTACCATT 60
CTCACAGTCC CTTTCAGGAA GCTACTCCGT GAAACCCCCA TGGCTGTGAG AAGTCTTTGA 120
CTGGAGGACT CTCACATCAT ATGCTACCTT TGCCAGTCCC GCCCACACCT GCGAATCAGC 180
TGCCAGCACT GCACCTGTGA TTTCTAAATT GCCATCTCCT GATCTCTACG TAACCTCCGG 240
TTGCACATTT CCAGTTCCTT ACCGGATCTA CCCCACAAAG GTCCATATGT TCCTCAACGT 300
CTCCAAGACT TCATCTAATT GTCCTGCCTG CCACCCCCAT CTCTCCTTTA GCACTTCTAT 360
TTCTTATTTC CTAAGTCAAT TGATAGGATT GCAAGAAAGT TTGGGGTTAT CTTGGAATAC 420
TTCCCGACTC ACAACTCCTG CGCAGGTAAC CAGCCACGAA TTCCTATGAT TCTACCCCTA 480
AAACTTCTCT GAGATCTATA GCCTATTCTC TATCCCCACT GCCACTGCCT GAGTTGGGCT 540
TTTGCCATCT TTGGTAGAGA CTGTAGCATC AATATCCATA TCTAGTGCCT GCCCTGAGCC 600
ATTCCTGACT CTGCAATAAA GAGGAAGCCT TCTGACCAGT GAGACTAAGA TCCACCATTG 660
AAGAATGAGG AGGATATTTA CAGGACTTCC TTAAGCCAAT AAGCGTGATC TTGCTATATT 720
CCAAGAGCAT GCAGCTCATT TGAGAATGCT TCTCATGTAA ATGTCCGTTG AGAGAAATGC 780
AAACACAGCC CATTCACTGA TTTGCCCTTT GTGTTGTCTT TTCTAACTCC TTTTCCCTTA 840
TGCGTGGGTG GAGTGCTAAC AGCTGTACCA GGGAACAACT AATCCCATGG GCAACCCGCC 900
GCCAGGGTCC ATCATTCACA GAAGACAATC TACTGTTTCT CATTGTGCTC CATGATTCAC 960
CCACTGCAAG AGAAAACTAA CACACAGAGT GATTGTTCCA TCTCCCGTGG AGAGGGTCCT 1020
TATTATGACA GAGAAGTTAT TTTCTTTTCT GTGGTTTCTT AAGGGTTCTC TAATTGGGTA 1080
ACCCCCTGCT GACCCCCGGC TATGGCAGTT TCTATATTGA TATCTTTGTT CCACTGCTTG 1140
CACACTGAAG CCAGGAACGA GTAATTCAAA CCAACAGAGA GCATAAGATA ATGGGGCTTT 1200
TATAAACTAC TAGTGTTTAA AAGGCAATGA CCCTTTAAGT TCACTGGAGT TCTCTTCCAT 1260
TAAGAATTTT TCTCACCTGT ACACAACAGA TGGGGGATGC ATTACAGCCC TGTGTCTGCT 1320
CCGGACGGGA GCTGAGCTCA TCTGCTAGAC TTCATGGACT TGAACCTGGA CTGCTTTGGA 1380
GTTCATTCAT GTTCTACCCA CACTTGGATA ACAGCTCAGA ATAAGCACAG AAGCTTTCCA 1440
TTTTTTTGTT TTGAATAAAT ATGGGAAAGT ATAAAGGGTA ATGGGAAATA AAATAAAAAT 1500
ATGGGAAAGT ATAAAGGATA ATGTAACAAA AACCCATATT CCTAGAAATG GTAACACCTA 1560
|
