| Tag | Content |
|---|
EnhancerAtlas ID | HS053-29052 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr4:6697180-6698610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr4:6698591-6698606 | GCTGACCTTGAGCCT | - | 6.9 | | Stat6 | MA0520.1 | chr4:6698282-6698297 | CATTTCCTGAGAACA | + | 7.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32360 | chr4:6693831-6699251 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTTCTTTTT GAGCTTAACA TTACAACATA AATTCTCAAA CTCTGATGTT CATTAAACAC 60
CCCAGCCCCA TCCTGGGAAC TTGGGCTTGG GGCTCGGGGT GTTCTGATAA TGATCAAAGT 120
ATGAGAATTG AACCCATGAG GACTTTGATC CAAGATACTG GGGTGTGGGG AGGGGCAGGC 180
ACAGGTGTCC TGGGAACACA CTTTGAGAAG CAATGGCAAA GCTGGGGGTC CAGCTAATGT 240
GTTACATTAG AATCACCTCG GGGAGGCCCT GGGTGCCCTT CTCAGCCCTC CCTCCGGAGG 300
CTGCTGAAGC CCAGCAAAGC CGGAGTCAGA GAACAATGTC CGCCTGAGGG CAGGGCTGGG 360
CTGGGCTGGC CTTCTGGCCC TATCTGCTCC GTGCCCAACC CAGCGCCCCG CACAGTCGGA 420
GCTTTGTAAA TACGAGGTGA CTGTCTGCCT ACAAACTTTG TAAACATCAC TTGAAATGGC 480
CGCAGGGTAT TGTGACATGG CCATACCACT ATTTGTTTGC TATTGAATTT GTACTTCCCT 540
GCCTTACTTT TGCTATTGCA AACCATGCTG TCACTAAGGT CTTCATGCAC ACAGTTGTGT 600
CTTGGTCAGA TGATATGTTT CTACCAATTT TAATTGTGTT TCTTTCCACC TGGACACACA 660
GCTCTCTGGC CCAGGGCTGG GTCATCAGCA CACCCTGCTG CTGCTGTTCA GATCTGCATC 720
CTGGTCCCGC TTGGTCCCAC AGTGAGAACG CTTTGCTATC ACATGGGCAG GCTCTGAGAG 780
CCCTGCCGGC CTGGCCTTCT CAAAGAAGAC CTGAGAGCTT GGGACCCAAG CAGAGAGGAA 840
GAACAGGGCT CAGGGTGCTT GCTCCATGCT CGCTCCACAC CTGGGGCTCA ACCCTGGCTT 900
TCCCCGGCTC CCTGTGTGAC TTCAGGGCAG GTCCCTTGGG CCCTCTGGGC CTTATCATCT 960
TCATCTGTAA CAGGGCGATG CCTCTGCCGT GTCTGGTGGT GTTGAGGAGT TCCTGTTTGT 1020
GTAAGCAGCT AGTTCAGTGC CAGCACGAGA TGGGAGGCCC ATGAAGTTAG CAGTGCACAA 1080
AAAATAGAGC AAAGACTGGA TGCATTTCCT GAGAACAACC ATCACTGTAA AGCACTTTAC 1140
AAATCCAAAG ACAACCCCCG GCAAAAACTC AAAATGAAAC TCCCTCTCGC AGAGCACAAT 1200
TCCAATTCGC TCTAAAAACA TTACAAGTTA GTTCATGTCA TGCCAGATAG CTGAAGGCAG 1260
CTCACAAGTT CTTAAGGCCA GGAATGCCAT GTGTCTGCTA TGCACAGCTG GCCCTGGCCC 1320
TGACAGCAAA GGTGACGCAG ATGTGGGTGC CCTGCTCCTG CCCAGCAGCA GTGCTTGGTG 1380
GAGGCTGAGG CCCTGCACAG GCACCCTCAC TGCTGACCTT GAGCCTCTCT 1430
|
