| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22225 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:45688240-45689630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIB | MA0081.2 | chr3:45688820-45688832 | AAAGGGGAAGTG | + | 6.07 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_13455 | chr3:45687708-45689949 | CD34_Primary_RO01536 | | SE_38488 | chr3:45683951-45689942 | HUVEC | | SE_42193 | chr3:45683990-45689611 | Lung | | SE_45221 | chr3:45683807-45689746 | NHLF | | SE_45828 | chr3:45682188-45690162 | Osteoblasts | | SE_56181 | chr3:45683821-45690421 | u87 |
|
| | 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 |
| GH03I045638 | chr3 | 45680304 | 45689900 |
|
Enhancer Sequence | GCATTATGGC TCACTGCAAC CTCTGCCTCA TGGGCTAAAG TGATCCTCCC ACCTCAGTCC 60
CTTTAGTCCC CTGGCTAATT TTTTTGAAAT TAATTTTTGT AGAGTTGGAG TCCCACTATG 120
TTGCCCAGAT TGGTCTCAAA CTCCTGGGTT CAAGTGATCC TCCCGCCTTG GCCTCCCAAA 180
GTGCTGGAAT TACAAGTGCA AGCCACAATG CCCGGCCTCT AAATCTTAGC CAGAGTTCAC 240
TTATTAGTAG GAAATTATTC ATGAAGTTTC TTGTTTTTGA TATTTTATAC ATCACCAAGT 300
CAATGTAGTC ACATTGTCAA AAAATGTATA TGGGAGAAGA AAATCACCTA TAATTCAATA 360
CCAAAAAGAA CCCCCAAAAA TGTATGCTGT GCCTACATAG ACGTTTTTGC CTGGTTGTCA 420
TCACAGTGTA TGTTTGCTTT TATGCCCTGC TTTTTCCACT TAGAAATATA TCATATGCCT 480
TTTCCCTCAT TGCTTCATAG TCTTCATAAC CATCTGCTGC GTAAGATCCT GTTGATTTGA 540
TGACTCAAAG CCAACATAAC CTTCTTGCCA GTTAAAGTTT AAAGGGGAAG TGAACTCTTA 600
CCATGGGAGC TCCCAGACTC TTCCCAGGAG TACTGAGGCT GGCTGAGTGT GGATCCTGTG 660
GCCAGGTTTT CAAGGACCAG ATGCATAGCA GGGCACGGGT CAGCCTGGGG GTCCGGCAAA 720
TCCAATGCCT GGCCAGAGGA TGCAGGCCCT TCCCTGTGTT CAGGGGCAGG GTGACAGCTG 780
CCTCTCCACA TCCGCAGCAG CCCTGCAATG GTCACCATTG GTGGCATTTG GATGCCAGCA 840
GGGTCCCATA TGCCCTGTTT TGGGCAGAGC GTCTCTGTCT CTTGCATGGA TCACTGCTGT 900
CACCTCCAGT CTGGTCTCTG GGCACAGCAG CGAGGAGGCC ACTCCACAGC TCAGAGACCT 960
TCAGCTACTT TTTGCCTTAA CATTGTAGTC CAGTTCTTTT GCCTGGTGTT TAAGACATTT 1020
CCTTAAATTA GTTCTAACTT CCTTCCTGTC TTCTTTCTTT CTAACTATCC CCCTCCTCCG 1080
CTGCCCCACA GCCTCCCGAA GTGCTGAAGT CCCTGGCCAC ACTGCACATC ACCTGTCCTT 1140
TTCTACCCCT GTACCTTGTC ACCCTTAGCC TCCATCACCA CCCAGGTGAA TATCACTCTC 1200
CCTTCAGTGT CTTCCATTGC CATCTCCATT GCTACTCTCC TGATCTTGGG TCCCATGTGC 1260
ACCCTTCATT TGCCTGTCCT ATGGTGTTTT CAATTATGAT TAGATTGAAA CTGTTTGCAG 1320
GAATCTCTAT CTCCCCCTAG GTGATCAGTT TTGGGAAAAA TAGGGACAGG GTTTAACTGA 1380
TCATGATTTT 1390
|
