| Tag | Content |
|---|
EnhancerAtlas ID | HS133-24219 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr4:120671160-120672460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr4:120672021-120672032 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr4:120672021-120672032 | GGGTGACTCAG | + | 6.02 | | SOX10 | MA0442.2 | chr4:120671478-120671489 | GTCTTTGTTTT | - | 6.14 | | STAT1 | MA0137.3 | chr4:120671399-120671410 | TTTCCAGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr4:120671399-120671413 | TTTCCAGGAAAAGA | + | 6.56 | | ZNF263 | MA0528.1 | chr4:120671732-120671753 | CTCCTAATCTCCTCCTCCTTC | - | 6.17 | | ZNF263 | MA0528.1 | chr4:120671738-120671759 | ATCTCCTCCTCCTTCTCCCTC | - | 6.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I119750 | chr4 | 120671765 | 120672634 |
|
Enhancer Sequence | GGATTTGCGG TTGTATAAAC CACATTTATT TGATTGGGAA AAAAATCCAT TTTGATCATT 60
TGGTAGTAGG GTTTCATCAA ATATCTTCTG TGCTTTAAGA GTTTATGTAA GAAACTATGA 120
GAGTCTGTTT TTTCCCCCCA ATTAGGACTT TCAAAAGCTT ACTGAAAAAC ACCCTTCTAA 180
ACTTGACAGC CATTGAGAGC TGTTGTGCTG AACTACAATT AGCACTGTTA ATAATAGCTT 240
TTCCAGGAAA AGAATTTAAT GACTATGCAG AATCAAAAAC TCTAAATAAA GTATCATTGT 300
GTATATCACT TCAATGTTGT CTTTGTTTTC CATGTAATAA ACAGGCAGAA AAATTGGTTT 360
CACTGCTAAA TACTATAACC TTTGAAAACA CAACTCTAAA AATATATTCA TTCATTCATT 420
CCAATGTGCC ACACTGTTGG TTACACAGAG GCCATAGAGA GCTAGGAACA GAATTTCCAC 480
TAGTTTTTTT TTCCTCTTTC TTCTGCTTCT TCTTCTCCAT CTCCTTCTTG TTCTTCCACT 540
TCTTCTCTCT TTCTCTTTTT CTCACTTTTT TTCTCCTAAT CTCCTCCTCC TTCTCCCTCC 600
TACCTCTTTC TCTCTCCTTT CCTCCTGCCT CAGGCTGCCA GCGAGAGATG CCAGGCCATT 660
TCTACATGCT CATTTCTGCC ACTAGCGAGA TCATACTGAG GCAAAATATA GAGGGATAGA 720
GATGGTTTCT ATCCCTATGT TCTGTGTTCC AAACACAGAA ACAAGCACCT TGTAAGTTAA 780
AGCTTACTGA CTCCTCAAGC CAATCCTAAG AAATAGGTGC ATTTTACAGA AAAGAAAACT 840
AAGATCCCAA GAAACCATCC AGGGTGACTC AGTCAGTAAA AGGCAAAGCC AGAATCATAT 900
ACAAGAGAGT AGAATGTGGC AGAAAAAGCC CTGGGCCAAG AATCCCAGGT TTGAGCTTTT 960
GAACCACTAG TCATCAGCCA TGTGGCTCTG GGCAGTCATC CACACCTCTG TAAGCCTCAC 1020
TACCCACTTG ATAAAATTAG AAATCTAGAT TCGTCATTTG TGAGATGTTT TTCTAGCTTT 1080
GACATCTTGT TATTCAGTGA TGCCCAGTTT CTTTATCCAC AAATCCTCTT AATCCTGCTA 1140
TTCATAGACT CTCACTCCCT TTTTAGATTC ATACATTGTT TTGTTTTGTT TTGTTTTTAG 1200
AGACAGGGTC TTGCTGTGTT GCCCAGGCTG GAATGCAGTG GTGTGATCAT AGCTCACTGA 1260
AGCCTCAAAC TCATAAGCTC AAGCAATTCT CTTGTCTCAG 1300
|
