| Tag | Content |
|---|
EnhancerAtlas ID | HS133-12796 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:46992040-46993430 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr17:46993323-46993344 | ATAGTGAAAGAGAAACTTATG | - | 6.58 | | MEF2A | MA0052.3 | chr17:46992751-46992763 | GCTAAAAATAAA | + | 6.04 | | MEF2C | MA0497.1 | chr17:46992749-46992764 | GAGCTAAAAATAAAT | + | 6.18 | | Zfx | MA0146.2 | chr17:46992146-46992160 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_64799 | chr17:46991190-46992214 | NHEK | | SE_64799 | chr17:46992249-46994381 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I048914 | chr17 | 46991385 | 46994389 |
|
Enhancer Sequence | AGAAAAGGAG AAGCTGCCCT GAAATTGAAA ATTTGCCATA AAGAATCACA GAGTAGAAAA 60
TTTCAGCCGG GTGCGGTGGC TCACACCTGT AATCCCAGCA CTTTGGGAGG CCGAGGCGGG 120
TGGATCACCT GAGGTCAGGA GTTCGAGACC AGCCTAGCCT GGCGAAACCC CGTCTCTACT 180
AAAAATACAA AAATTAGCCA GGCATGGTGG CGCATGCCTC TAGTCCCAGC TACTCGGGAG 240
GCTGAGGCAC AAGAATTGCT TGAACCTGGG AGGCAGAGGT TGCAGTGAGC CAAGATCACG 300
CCACTGCACT CCAGCCTGGG TGACAGAGGG AGACTTTGTC TCAAAAAAGA AAGAAAAGAA 360
AATTCTTAGG TGTTCCTAGT TGACTGTATT AGCTTTATCA GCCATGTTTT TTTTTTCCTC 420
TTTACCTAGA AAACAATGTT GGGCTGACTT ACTGACAAAA GAAATTTAAC GAGAGTTGAC 480
TCTGTTGTAA AGCTTCAGAG AGCAGTAGGT CTAGAGTTCC TGGGGGAGCA AAGCTGAAAA 540
GATAGAGGCA CTTAAGAGCA GTCCCCAGTG AAGTTACTAT TAGGCATTAC TGACTTGGGC 600
TTTCCTCAAG TACAGCAGGG AAACAGAAGC AGGCAGTCAA CTTGAACAAG CCAGTCCTGG 660
CTTAGGTTGT GTTCGGCTTC CAGCTCCGGT GCCATCTCTT CAATTAATTG AGCTAAAAAT 720
AAATGTCATT AACATCCAAG CTGTCCCCTC CCCCTAATAC TTGGTTGGGT TTATGAAAGA 780
GAGGAGCAAT TTTGGTATTT GACGTTTTCC ATATATTATT TTCAGACCTT CCACTGTCTG 840
GAAGCACCCC TTATTCTCTT CCTGTTCTTT GGAAGAGTTG TGTAGTCTTA AGAGAATTTG 900
ACACTCCTTG GGGGTTTGAT ACAGAACTGG ATCCCCAATA GCCCCACCAC ATGGCCTCTA 960
ACCAGATGGC TTCAGTCACC TGTGTCCCTT TATGCTCAAC TTCCCTCTCC CCTCACTAAC 1020
TCCATCACCA CCCATAAACA AGCTCTTTGA GATCCACGGA GATTAACATT TAGACAACTT 1080
TGGAGCTAAT TGCTTACCTA ATTTCTTTTG TTTTGATTGT CGTAACTGTT TCTAGTACAA 1140
AGAAAATCCC TTCAAAGTTA CATAGCTTGC TATTACCTGT TCTTTTGCCC CCCCCCCTTG 1200
ATTTGAGGAT TAGGCAATTG ACTGATTTCT GGTGAAATCA GAACATGAGC ATGAGACAGA 1260
GGCTGGGAAA TTCCAGAGTA TTAATAGTGA AAGAGAAACT TATGGTGAGT CACTTATGGT 1320
GGTGTTGCCG GGCCCCAGGG TACTTGTTCC CTATTCTTTC TCTGCCTCAC CCTCCATTCC 1380
TTCTGATGTG 1390
|
