| Tag | Content |
|---|
EnhancerAtlas ID | HS102-14870 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr21:38160000-38161220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr21:38160518-38160528 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr21:38160518-38160528 | GGCACGTGCC | - | 6.02 | | NFE2L1 | MA0089.2 | chr21:38160578-38160593 | TCATGACTCAGCTGT | + | 6.11 |
|
| | 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 |
| GH21I036787 | chr21 | 38160210 | 38161040 |
|
Enhancer Sequence | GCCGCTCGAC CATGAGGATA TTCTACAGAA AGAGAACTCA GCTCTCTCCT TCCTACCTCA 60
CATGACCCTA AGGAAAGTTA AGAAAAGAGG AAAAGACCTG TGAAGATGCC TGATCAGCTG 120
TCAGGGTTAC GTAGACACTG GCTGCTGTTA TTTACTGTTC CCTGGCTGAT AAAATAGCCA 180
GGTCACCTGT GCCGATGACC AGACCCACCC CCTACCCACC AGCAGGGCTG CCAGGGCTTT 240
CTGGGGAGAC GCTGCAGCTT GGTTCTTATT TCCTTTGCTC TGCATCCCTC TGGGTTGACT 300
TGAGTCTGAT CATGGGTTTA TTCCATTTCC ATTTTGCTAG ATTCCCTCCA CTCCCTCAAG 360
CTTCTACAAA ACTGTGGGGC CACCACTCCC CACAAAAGAT TAAAACCAAG ATGTTTCCTA 420
GAGGTGGCAT TTTGTCTTCC TGAAGCTGTT CTGTGCACAG GTCCTCTCCA CACTCATGCC 480
AAATGCTCGG TGAAGCGTCT TCCTGAATGT CCCTAAGGGG CACGTGCCAC TGGCAGAGCT 540
GATGGGCACA CCTCACTCCC ACACATGCTG TGCCGAGCTC ATGACTCAGC TGTGCAGGGC 600
CCGCCCAAGA GTGAGGCAAA CACCAACACC GCACAGCGAC CCTTTGTCAA TGGTGGGGAC 660
CTCAGTGGCT TCTCCATCGG AACTTAGGGC TGACGGGCCT CCAGACCTAC TGTTACACAC 720
TGGCCCACGG AATGACCCTC ATAAACCCAA GAACAGTAAA CAGAGCTTAA CATTCTAACG 780
AAATCAAGAT TGCTGTGTGT GCTTTCACAA AATGAAACTG CCTGGAACTT CTCATAACGT 840
TTTTTATGAT AAGCATTAAA ATGCAAAGAG GAAGATTAAA GTTCCTGCTA CAGACCAGAG 900
CAGTAATGAG TGTGGGAGGA GGAGCTCTGG GTAGGGTCTG GGAGAGAGGT TTATGTACTG 960
CATTACAGTT GGATATTATT ATATAAAATG AGTGTGTTAT TAAAAGGATC CTGAAGTTAT 1020
AAAAACTCAA AGGAACTTTT ACTGAGGATG AATAACTTCT TTGGTAAAGA TGAATGACTC 1080
TCACGTCCTA GACACTGAGG TGCAGTCACG TGCCAGAGCT CTTTAATTGC TAGTAGTTGG 1140
ATTTCGTTGT TTTTGTGGGG CACTTTTTTG CGGGGGAAGG GGCAGAAAGA TTAGGAATAC 1200
ATTCTTTGAT TAGGAAAGTT 1220
|
