| Tag | Content |
|---|
EnhancerAtlas ID | HS133-27282 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:106567030-106568660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr6:106568563-106568574 | AGGCCATAAAA | + | 6.02 | | YY1 | MA0095.2 | chr6:106567222-106567234 | GCTGCCATCTTG | - | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27341 | chr6:106566742-106567893 | Esophagus | | SE_58834 | chr6:106530700-106671989 | Ly3 | | SE_62631 | chr6:106531123-106575028 | Tonsil |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I106119 | chr6 | 106566886 | 106568680 |
|
Enhancer Sequence | AGATTCACTC TGCCATGAAT ATTCATCACT CACTATGGGT CATGATCACA AATGCATGTC 60
CTCAGCACTC TGGCTGGGCT TCAGCAATTT ATGGAGTTGT TATTTGCACC ACCAAACCAG 120
TCAGGAATGA AAATAACAAT CAACTCCTTA AATGTTTACA AGCCTCCTGG GCTATTGCAC 180
ATGTAATTTA GAGCTGCCAT CTTGTCTCCT TCTTTCTGTC AGTGGAATGG AATGTCCCCT 240
CCAGTAACTT GTTGGCTTTA GGAACATGGG GAATAGAAGG CTCCTCAACC TGAATTGTCT 300
AGTCAAGGCT TGGCTGAAGT CCTCTTTGGT AGCAAGGTGT TTGGGTTCTC ATTGCTCTGC 360
AATGCTTCCT TATACAAGTC ACTTGAAAAC AAACCTTCCC CGCAGGTTGT CCTTGGAAGC 420
AGAGCAGGAG GCAGGTAAGT ACTCTCACCC AATCAGCACA ATCAATTTGT CATTCCCTGA 480
AAATAGAGTC GTCCCTCCAG TCTGTCCAGG TCGGTGGGGA TAGAGAGGAA GGCCCAGCTG 540
CCTTTGAGCA ATGCCACATT CCAGTGGGGA GTGGTTCCCC CACATTCACC GCACTAGGGC 600
GGGCGTGTTG TGCCTCGTGC CTGCAGCCAC CCTTGAAGTG TTGTTGTTAA ACAACAGTCA 660
TGAACTCTGG AATGTCTCTG GTCATTTATA GCGTGACTGT GTCACTCTGT AAATGACACT 720
GTCAAGCTTC AAGGCCTAGA ATGAAGTTGG TTTGCTTTTC AATAGATCAT AGTCCCGCCC 780
AAAACAAAGC TTCCAGGCTT TTACAATGTA CTTCTTACTC TGAAACTCCT AAGAGAATAG 840
AAATGCTAGG GAGATAAAAT ACAGGAATAG ACTACAAATC ACACTCCAGT CATCTTACAG 900
GCCCTTTAAA ACACATAGAA CAATTTGACC ATACTATTTG CAAATAAGCA GCTTTCTGGA 960
AATTAGCTGG GCTCTTCTTA AAGCAATTTT TGTCTTCTCT CACCCTTGTC TTGACTTTTC 1020
CTTCTTTGGT TCATTTCCTT CATGAGATAA ATGAAGAGCG CAAGAGATTG AGGTTCCAAA 1080
GAACATGTGA TTCGTGAGTC ATGTCTATTT TTTCTCTATA GTGTTCATTG AAAATTCATT 1140
GTTCCAGTAG AAGAAACAGA AAGTTAAAAT GAACATTAAA TACTGCTTTT GCTATTTCTG 1200
TAATACAGCA ATAATTATGA AAATAATGCT TCTCATTTGA TTTATGCTGT ATAAGTTACT 1260
ATGGTCTGTT GGTCACTGTC TCATTTTATC CTCACAAATA CCCTCCGAGA TAACTTTATT 1320
ATTTCCATTT CGTATACAAG AAAACTGAGG CCCTGCGAGG TCAAATAAAT TAGATAATGC 1380
AGGAAAAAAC CTTAACCCAG TGCTCATACA AAATAATCCA CAGTTAACAT CTTTAAGGAA 1440
CTTGCTTGAC ATCACACACG TAGGAACTGT GATGAGGACT GTGACCTTCA TATGCTGTGG 1500
TCAATACTCA CTCCACCTCA GCAGAGCAGC CTTAGGCCAT AAAATACACA GATATTTAAA 1560
GAGAAATATG GTTTTAAACC TATTCTGCAA CCTACAGCTT ATTATGTACT AGCTATGAAG 1620
GTAGGTTTGT 1630
|
