| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02638 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:159774160-159776380 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PPARG | MA0066.1 | chr1:159774720-159774740 | AGTGGGTCAACATAACCTTC | - | 6.06 | | RREB1 | MA0073.1 | chr1:159776134-159776154 | GGTGGTTGGGTGGTTGGGTG | - | 7.05 | | TBX21 | MA0690.1 | chr1:159775266-159775276 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr1:159775265-159775276 | TTTCACACCTT | - | 6.62 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I159803 | chr1 | 159773668 | 159775133 |
|
Enhancer Sequence | CATCTTTCCC AGATAAATAT CTCCCGATCC CTCAGAAACT TTAAGAGGAA ATTATCCTGC 60
TCCTAGAGTT GGCAGGGGCT CCTGCCTTCA TTTTTCGGAA TTCTATTACG CAACTTGGTT 120
TGACCATAGC TCTTGGCCAC TTCATGATAC TGTCACCTCA TCTTCAGCCT ATAGCTAATG 180
GAGGTCCCTG GGCCCTCATT GCAGGAACTG CTGTAAGCAG GTGTCACCCC CTGTGTATGT 240
TCCCAGTTGG CTGCTGTTTT GATTGCAGAA ACCAATTTTG TAATCCCACC TCCAAGATCT 300
TGCAGTACCA TGGGGAGCAA GTCATTGAGA TTTGGGGACA GGAGCTCATT TTAAGTGCAT 360
CTATGCTTCC TGAGTGCCTT CTGTCTTGTT TTTGGCTTCA GTAGTCTCAA CCCTGTTTGT 420
TTAGCACTTT GTAGCTGCAC AATTGTTTTC CAGTGAGGTG GGGAAGGGAA GGAAGACATA 480
ACTACAGAGT AAGGTCTCTG TCACTCTGAG GTCAGGCCTT CTTTCTGCTT TCAGTTAATG 540
TAGTAACCAC TTTCCCAGGC AGTGGGTCAA CATAACCTTC ACAACTACAC TGTAAGAAAA 600
AAATGACTAT TATCATTTCT ATTATGTGAT ATGACAGAAT GAGATATTGA AGGCTCTTGG 660
AACTTAGACA ACTTGTTCAA GGTCGTACAG AAAGAGGCAA ATTCATGACT CAAGTCCAGG 720
TCATCTGATT CCAAATCCTG CATGCTTTCC ACTACACCGA GCTCATAGAT GGGGGTTAGG 780
GGTGGAGATG GAGGGATGAT AAAGAAGAGA CTCATTGTTC TGCACACTCT TGAGAGCATA 840
TGACTGAGCT GACCCTGAGC TGAATAGAGA ATTGAGCTGA AAGATTCCAC CTGTGTCCAA 900
AGTAGTGTAG AAAGCAAAGA TGATACCATG TGACAGAGCC AAACATCTGC TCTTAGAGGG 960
TTTTCACCCA CCCTTCCCAA GGCCATTCTT GCATTTTTTT TTTGGTGTTA TGTAAAATAC 1020
CTAGGACATG CCAGCAATGC AGGACACAAG TAAATGTATG AGGATTGGCT GGACTGACTG 1080
CACTCAGCCC TACATTCATT CATTGTTTCA CACCTTGCCC CAAAGTCCAG AAGATTCTTC 1140
ACTGCTTCAT ATCCAGCTAT GACCTTCAAT TTCAGGTCTT CCATTGTTTG GGCTATTCAA 1200
ACCTATCTAA CCATATCTGT CATCATTTTG TGAGTTGGCC CCTCTTCCCA GGTCACCTGT 1260
TCTCACACAT TCACTCATTT AAAAACATGA ATGTAGCACA TCCAAGATGC AAGCATGATG 1320
TGGGATGCAT CCAGTTTGTT TGTAGTTCTC TCATTCATCC ATGCTGCCTG ATAATGTCTC 1380
ACATCCTTTA ATGATTACTC TTTCAGGGGA CTTATCCTCC TCAGTCTGGT CACTTCCATA 1440
CCCTTTTTGC CAGAGCTCTG TGGAGAGATG GGACCACAAG AATCAGGTCC TGCCCTTGCT 1500
ATATGGGTTC TCCTGTAGAT GTTGGAGGTA GGACCCTCAG GCACATTCGT ACAAGAGTCT 1560
AGTCCTATGT TTTCTACTTT TTGCTTCCCA CCTCGTACAA TGGGATGCAA AGGAAAACAT 1620
TCATGCATTT ATTCAGCAGA TGCTTACTGA ACACAGACTA TGTTCCAGGC ACAGGTCTTG 1680
GGCATAGAAA ATATAGCAAT GAGTAAAATA AGCAGAGTCC CTGCTACTAT GGAGCTTATA 1740
TTCTAGCCAG AGAGAGAGGT GATAACATGT AGGCAATTTA ATGAATAAGA TAAATTCAAA 1800
TAGTGATAAG TGTTTTGAAG ATAATACAAT GGGGCATTGT TTTAGTGATT GGGGAAAATT 1860
CTTTTGATTG GAGTCCCAGG GAAGACCTGT TTGAGAAGGC AACATTTGAA CTGTGATAGG 1920
GCAAAGAGTT CTAGGGAGTA CGTCCAGCAC AAACGTTGAG TAGTCAAGTG GCCGGGTGGT 1980
TGGGTGGTTG GGTGGTTGGA TGGTTGGATG GTTGGGTGGT TGGATGGCTG ATGGCTGGGT 2040
TGTTTGGTGG TTGAGTGGTT ATGTGGTTGG ATGGTTGGAT GGCTGTGTGG ATGGGTGGCT 2100
AGGAGGTTTG GTGGCCGGGT GGTTGGTTGA ATGGGTGTAA GTCCCCATTG CTGAAGTGAC 2160
AGGCCTCCTT GTCAGAAAGC TCTTTTTGCT ACTTAACCTA ATTGTGTTAC TTTGTTCTCT 2220
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