| Tag | Content |
|---|
EnhancerAtlas ID | HS133-30922 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr8:101998250-102000560 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr8:101998703-101998714 | TTTTATTGCTT | - | 6.32 | | FOXP2 | MA0593.1 | chr8:101999710-101999721 | AAGTAAACAAA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH08I100985 | chr8 | 101997949 | 101999804 | | GH08I100988 | chr8 | 102000421 | 102000570 |
|
Enhancer Sequence | TCAGATTGTC CCTCCATCGC CCCACCACCA CCAAATGACC AAGCCCTTTT TGAACTCTGC 60
TATTTTATCT ACTTCAATCT AAAAGCATCA AACTTCTCTT TGCCTCTGAC TTTTACACAC 120
ACACACACAC GCACACACAC GCACATATGT ACACAATGAC TCCTTAGTTT CACGTGGATT 180
CTTGTAATTC CATTGCACTT GGTCCATGTT TCTGATACTG CACTCATCAC GTTGCATTTC 240
ATTGTCTGAG CCCTCACGTG ACAGGCAATG TTCAGGTACT AGGGATTCAG CTATGATCAA 300
TACATGAAGA TCCCTCCCTC ATGGAACTTG GATTCTAGTT AGAAGACTGG TGAGAAAATA 360
TAGGGCCTTT CAGAGGGTGA GGGGCGATAG GGAGAAAAAC AGTGCAGGGG GAGGGTAGGA 420
AGCACGGGGG AAGGGAGGCC ATCTGATGGG CCTTTTTATT GCTTGTTGAC TCATGCGCCT 480
TCCCAAGGAC ACACACCAAG TCGGTCTTGG TTTCTTGAAT TAATCATCTT TCTAACTGCC 540
AGGCCCTGTG AGGCTCAAGA AAGATTTGTT GATTGAACAC AGGAGAACGA TTTCATTGAG 600
CTCATTTGGT CTACAAATAG TTTGCTTTCC ACAGCTTTTG ACAAAAGAAG TGTTCGTTGT 660
TACGACTCAC TAATGGCCCT TCTAAGAAGG AAGTGACTGT TTATTTTTGG GGTGGGTTCT 720
CTGCTTTCCA TGGTTTTATC AGGGCCCAGT GTACCCTGGC AATTTTGAGC AGAGCTTCAG 780
CACAAGCCCA CAGAGAAGAA AAAATAGACA GTCTTGGTCA GCAAGGAGGA AACTTATTCC 840
TTTTATGGAA GAGATTAGAC ATGGGAAATT AGAAGGCAAA AAATAATGCC AGGGGCAGAA 900
AAGGAGACAT GAAAAGGCAG TGAGAAGAAG CAAGGAAGAT ATAGCGAGGG AAAAAATATA 960
AAGGAAATGA ATTGGTAGAA AAAGCCAAAG CAAGGATAGG AGGAACCCAC AAATCCCCAA 1020
CTCTGAGGAC GCTGGAGAAC TGGAAGGAGG ACCACAGGGC AGGGAGAAGG AGAAGCTTTC 1080
AAGAGTGAAC CCAGGCCAAG GAATCTCAAT TTATTTCTAT TTTCAATGAC TATAAGTATC 1140
CCTGAAAGTC TGGGGAGATC TTAGGTCTCC TCCCACTGGT ATCACTCTCC CATTTAATCT 1200
TCACAGTCCT CAACATCAGA AGGATGCACT TCCAAGAGAA GCGCCTCAGA GACAACCCTT 1260
CTAAGTGCTG GGTGAACCTA GACTGTGCTC AGTGCAGTGG GTTCCAAATA GTGCCAAAGC 1320
CAAGTCCGTT CTCGTGAAAG TTAGCAGTGG AAAACACAAA AAGGCCATGT GAAATTTTAC 1380
TCGATCCATA AGGAAAACTT TGGTTATTCC CCATGAAAAT ACTCCTCAAA GCCTGTCTTT 1440
ACCATACAGA CTAAATAAAT AAGTAAACAA ATAAGCTGAG GGTGGTGGTG TGAGCCTGTA 1500
GTCCTAGCTA TTTGGGAGGC TGAGGTGGGA GGTTCACTTG AGCCCAGAAG TTCAAGTCTG 1560
CAGTGAGCTA TGATTGCACC ATTGCACTCC AGCCTGGGTG ACAGAGGGAG ATTCTCTCTC 1620
AACAAAACAA AACAAAAAAC AATAACAAAA AAACTTCAAA AACAAAGAGT CAAAAGCCAA 1680
AGGTGTGGTC TCGTTCTAAA GACTTCATGG CAACTTGAAT TTTGGTGTCT GTCTTACAGG 1740
GGCTAAGGGT TCTTGTCTAT CTATGGTGGC ATCAACCACT CCTGCTTTTT GATGCCTCAT 1800
TATCCTGGGA GAAGGAGAGG CGAAGAAATG GCAAGTGATT GCCACTAAGG TGGCTGCAAG 1860
TGAATGGCAG TTGAGAGCCA GGCGGTGGAG CCTGGAGGTG AGTGTAGGTA AGCACTGATA 1920
AAGGCTCCAC ATTGCCCATG TCAACATGCC AAAGGCACCT GCTCATGGTA GTGCTTACAT 1980
CCTCTCCCTA AGATGATACA TCAAGCCCGA GATCCCTAAG AAGCTCTCAC AGCCTCTCAG 2040
AGCCATCACC ATCTGCAAGG GACAGGGACT AGCCCTTACT GTCTACTATG AATTTATTCC 2100
AGTAAAACCA AGTATTTTCT CTTTTTTCAT TCTCATATAA ACTCTAGGAG TAAATGAAAG 2160
CAGAAAGTTG TCAAGCAATT TGCTTTGGGT CTCACTGCCA ATAATTGCTG GAGTCTGAAC 2220
TTGAACATAG CCCTGACCTT TTGTTTGTGC TCTTCTCACT ACAGTGGCTA CTTGGTGGTA 2280
TTCACATGAA GGCAACAGCA GAGCACTGAG 2310
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