| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01132 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:32139180-32140600 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr1:32139431-32139446 | GGGTCAGCATGCCCC | + | 6.3 | | Klf1 | MA0493.1 | chr1:32140214-32140225 | GGCCACACCCA | + | 6.62 | | LHX6 | MA0658.1 | chr1:32139795-32139805 | ACTAATTAGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_08709 | chr1:32138479-32139781 | Brain_Inferior_Temporal_Lobe | | SE_37280 | chr1:32134690-32141924 | HSMMtube |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 32139536 | 32139641 | | chr1 | 32140302 | 32140543 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I031668 | chr1 | 32133986 | 32141576 |
|
Enhancer Sequence | TTTACTCAGC ACCCATGACG CTGGGCATTG TACATAATAA GCCCTGCACA TTATCACATG 60
CCATCTTGAC GGCGCAGTGA GACAGGGAAT CTTATAAGCA TTGTGGAGAT GGGAAAGCCC 120
ACTCAAGAGA GGCGGCGTGA CTTGTCTAAG GAAAGTGGGA GCCTGGATTG GCGTGGGCCT 180
GTCCTAGGCC ACAGCCAGTG CTCTCTCCCC AGGCTTCCTG GACTATGGGT GCAGGTGGTG 240
GCTGGGGCTC TGGGTCAGCA TGCCCCGGGG TGCCATCTGA CCCCTTCTCC ACACTATGCG 300
CACTTTCTAT TTGGAATCCT CTGAAGAGCA CTTGATGAAG AAGCCAACAG ATGAAATGTT 360
ACAGGAGAAA TGTCAAATCC TGGATTTGGA GTCACACGAT CACTGCCCAG TCATTGACAG 420
AAGCAGAGGG GAGAAGAGCT GGGGGTTTCG TTGCCACAAC CTCACTGTGA TCCAACATGT 480
AACTGATGCC AAGAGGTTAC CCCGACCTCC TCTGGCTGCT TCTGGAGAAA TCTGCCGTTC 540
AGAGCAGGGA AGGGGTAGAC AGCCCCCATG CTCTGCCCTG ACCAAGGCCC ATCGGGGTCA 600
TGGGATGTCC AGGGCACTAA TTAGCCAGTG TCAGAAGAGG GTGGCCAGGA TGAGGGGGGG 660
CTCTGGAGGC CAACACATGG GAAAGACCCC TGAGGATGCT GGGCTAGAGG AGAGAAAGTC 720
CAGGAACATA AGGGCCTCCT TCAAAAACCT GAAGGCAACC TGGGGAATTA CTGTGCTCTC 780
GTTTCTAGAG GTGACTAAGC AAAGATGGGC TATGTGACTC TTGATTCCAA TAGGAACTTC 840
TGCTCAGTTT GGGAAGCCGG CCCAGGCCAC AGCCCTCTGG TAGAGCATTA AGGCTGTGTA 900
CAGGCCCTGG CACAGGCCGA CCCTCTGACC AGGTCCGAAG TCCCCTTTCT TAGACTACCA 960
GAAGTGCTTC TCAAATCCAT CTCCTCCCTG GATTCTTTCT GGATTGACTA GAGAACAGCT 1020
GAAGCTTTCT TCCAGGCCAC ACCCAATCTC ACAGCCCCCC ACCACTGCAC TTTCACCCCC 1080
TCTGCTTTGC TTTGGAAGCT GCTGGGCTCT GCCGCAGGGT GACCCGGGTG CTACGGGGTC 1140
TCATTGCCAG CTGCTGCGGG CAGGCTTCAG GGCTGGGTTC TGCCGACAGC ATCTGCCATG 1200
TGGGCACCTT CACAGGATTC CTTTAAGCAC TCATTCAGCA AATGTTGCCT GGGGGCCTGT 1260
TACAAGCCAG GCATCAGCTA GGCCCTCTTA GACAGATGCT TGGAATGCGT ATTCCCTGCA 1320
AACTGCTGCT CTCTCTGCGA GGTGCCACAC AGCTGAGCAC TTACTAAGAG AATCCCCTTA 1380
GGAGACACCC CCGCCAGCTC ACACTTCCCT CCTGGGTACC 1420
|
