| Tag | Content |
|---|
EnhancerAtlas ID | HS133-16623 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:30336010-30337760 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:30337215-30337230 | TGACCTCTTGAGCTC | - | 7.14 | | RARA | MA0729.1 | chr2:30337212-30337230 | CCTTGACCTCTTGAGCTC | - | 6.71 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_68001 | chr2:30331536-30388030 | TC32 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I030113 | chr2 | 30336140 | 30338793 |
|
Enhancer Sequence | CCCTCTAGAG AACTCTAATA CAACATACTT TCGGGGTCTT GGGTTACTTC TCCCCTCTCC 60
TGAGATCTTA TGGGGAAGCT GCTGATCACC AGTTTCAGAT GTTTTCTATC TATTAGGAGA 120
CTGCCTTTCC CTGGTGCCAC TGTGAACAAT TATTACTTTA GAGAAATAGG TAACAACCAC 180
CTGACCCTCA CCTGATGGTC GCCCAGCACT CCTGGTGTGT GTTGGGGGGA GGCCTCTCCC 240
GCCCTGCTGA TACCTGACTA TCTGCCTACT GTCACACGAC TACTCGCCAC CACTCACATG 300
GCGTTTCTAT CCAGTCTGGA TCATTCCTGC CAGCCCTGCA GTTCAGGGCT GTCCTCAGCT 360
GGTGCCCTAT CAGACTTACA CCTGCAGGGC AGATGCAAAA GTGAAAACCT TCCTCCAGCC 420
CCACAGTCTA AGAAAAAACA GATTTGAGGC ATCAAAGGCC CACTCTCTGA AGGACCAAGG 480
CAACTGTGAG GTTCCACTGA AGCTCTGTGG TGAAGCCTCC TTCAAGCTTT CTCCTGCAAA 540
CCCCCTCATC TTCCACGCTG TGACTCCACT CCAGGCCACT GCTTTAGAGA CCTCTTCTAA 600
CCCGCTCCAA GGACATGACA TCAGGGCAGG AAAAGCGTGC CTTATGACTG GGCTCTGCCT 660
GGGCTTAGTC ATCCTGCTGG ACCAGCTCTA GGGGAAGGCT GTGGTTTTAC TTCATCTCTC 720
TGAGCTTGTA AAATTAATCA AACTTGTATT TTTAGTACAG GATTTATTTT TCAAGGTCAG 780
TTTTTCCAGA TCTCATAAAA AGATAAAAAG TGGTAACAGC TTCTTTGGAT ATCTTAAATA 840
TTCTACATGC AGAATGAAAT GCATCTTTGT ATAAGAAAAC CCTGGGGTGA GTATGGAGAG 900
CTAGCTCTCC CCAGCAGTTT GAAAAGCCTC CGGGTCACTG AGTGCCAGGC CAGCTCCACC 960
ATTCTCTGGG TTGATGAGTA TGTCTTGTGA AGGGCAGGGT GTTAATCGTT AACTCAAGCT 1020
TTTGAAAGGG AGTTCAGTAG CATAACTTGT TAGTAATGAA GGGGTGCAGG CAACTTCACC 1080
CCAAAATATG GCTCCTTGGT ATAATGAGGA TTTGGGGTTT TTTAACTTTT TTTTTTTTTG 1140
AGGCAGGGTC TCACTCTGTC ACTCAGGCTG GAGTACAGCA ACGTGATCTC AGCTCAGTGC 1200
AGCCTTGACC TCTTGAGCTC AAGAGATCTT CCCACCTCAG CCTCCTGAGT AGCTGGGACT 1260
ACAGGTGTGA ACCATCGTGC CCAGCTAATT TTTAAAATTA TTTTTGTAGA GATGGCAGTG 1320
GGGAGGGGAT CTCACTATAT TGCCCAGGCT AGTCTCAAAC TCCTGGGCTC AAAAAATCCT 1380
CCCACCTTGG CCTCCCAAAC TGCTGGGATT ACAGGTATAA GCCACCATGT CTGGCCTATA 1440
ATGAGTATTT TGAAGGCCCT TAGAGATCAA CAGATGCTAG AAGAGACTTT TATCCTATCT 1500
GCATAAAGAC CAGGTGAACC CACCAAGGAA AGTAATTGTT TTTCCTTCTT CTTCCTGTTA 1560
TCTTATTATC TATCCAATGT AACCACACCT GAAGAGACCC TTTCACAGGA TAACGTCTGT 1620
CTCTCAGGCT CATTCAATTT CCAGAGATAA CCATTTACAA GTTAATCTAT GTTCCCGATC 1680
CATTCATTCT CCCTAGTAAT CATTTCTTGC CTCTCAACAG AAGTACCTAT ATTCCCCATC 1740
TCCCCGCTTC 1750
|
