| Tag | Content |
|---|
EnhancerAtlas ID | HS179-12722 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr14:103893550-103894720 |
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 | chr14:103894216-103894231 | GGGTCTTTGTGACCT | - | 6.34 | | IRF1 | MA0050.2 | chr14:103893839-103893860 | AAAAAAAAAAAGAAACAAAAG | - | 6.21 | | RARA(var.2) | MA0730.1 | chr14:103894132-103894149 | AGGACAACCAGAGGTCA | + | 6.62 | | STAT1 | MA0137.3 | chr14:103893964-103893975 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr14:103893964-103893975 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr14:103893964-103893978 | TTTCTGGGAAAAGG | + | 6.15 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09869 | chr14:103893831-103896534 | CD14 |
|
| | 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 |
| GH14I103426 | chr14 | 103893282 | 103895765 |
|
Enhancer Sequence | AACAGGCCAG GCGCTGTGGC TCACACGTGT AATCCTAGCA CATTGGGAGG CCGAGGCAGG 60
TGGATCACCT GGGGTCAGGA GTTCGAGACC AGCCTGGCCA ACATGGTGAA ACCCCATCTC 120
TACTAAAAAT ACAAAATTAG CCAGTCGTGG TGGTGCGCAC CTGTAATCCC AGCTACTCCA 180
GAGGCTGAGG GAGTAGAAAC TATGAAAACT TGGGAGATGG AGGTTGCAAT GAGCCGAGAT 240
CATGTCACTG CTCTCCAGCC TAGGCAACAG AGGGAGACTG TTTCAAAAAA AAAAAAAAAA 300
GAAACAAAAG AATGGCTGCT CCATAGACAG AGCAGCAGTA TCAGCTGCTT GACTGAGTCT 360
ACTTATAGTT ATTTCTTGAT TATATGCTAA ACAAGGGGTG AATTATTCAT GAGCTTTCTG 420
GGAAAAGGGC AGAGATTTCC TGGAACTGAA GGTCCCTCCC CTTTTAGGGG ACTATTTAGG 480
GTAACTTCCC AAGGTTGCCG TGGCATTTGT AAACTGTCAT GGTGGTGGTG GGAGTGTCTT 540
TTAGCATGCT GATGCATTAT AATTAGCTTA TAATGAGCAG TGAGGACAAC CAGAGGTCAC 600
TTTCATCGCC ATCTTGGTTT TGGTGGGTTT TGGCCTGCTT CTTTACCACA TCCTGTTCTA 660
TCAGCAGGGT CTTTGTGACC TGTATCTTCT GCCAAGCTCC TCCTATCTCA CCCTGTGACT 720
AAGAATGCCT GACTTCCTGG GAATGCAGCC CAGTAGGTCT CAGGCTTATT TTACCCAGCC 780
CCTTTTCAAG ATGGAGTTGC TCTGGTTCAA ACACTTCTGA CATATTTCCC CCCTCCCTTT 840
TACAGGGGGA CCCTTAATCC TTAAGAATTG TAGCGGGACA AAGATCATCT GTAACTTCTT 900
CAAGCCAAAT AGGGGTGATG ATATTCCTGC CTATTAGGGT CTCTTGTATT TAGGGTAGGG 960
AGAAGTTTAG TTAGAAAGCA TTGTTATAGA AGCCCTTATT TTCAGTTACA CAATTTTATA 1020
AAGTTACAAT TGCTTATTGT AACCAGCTGA GTTTTAGGTT TTGTGGTTTG TTGCTTGCTT 1080
GCTTGCTTGC TTCTTAATGC CATATATCTT GGCATTTATC AGTCCATAAT TACTAAATTC 1140
TTAAAATCCA TAAATATTTA TTATTCTTTC 1170
|
