| Tag | Content |
|---|
EnhancerAtlas ID | HS176-19836 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:25049000-25050410 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr2:25050304-25050314 | GGTCACGTGC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH02I024826 | chr2 | 25049041 | 25049190 | | GH02I024828 | chr2 | 25049381 | 25049550 | | GH02I024827 | chr2 | 25049774 | 25051676 |
|
Enhancer Sequence | GGGCAGAGCG TGTGCAACTG AAAGGGCTGT CATCTGCCTC CTGGAGGGGG CCTGATTCCC 60
TCCAACTAGA TGGTGCTGCT TCCTGCCACC CCAGCCCTAG AGCTCACCCC GGCTCCTTAG 120
GCCCTTTCAC ATCAAGTCGG GCTCCCCCGG GCAGTAAAAT TTTCTTAACT CACTGGGCTC 180
CTCTCCAACA GCCAGGCAAC CCCTGGCCCC TCCTGGCTGC ACCTGGTATT CACATCAGGG 240
CTGCTCCCCA GGTATTTAAG AAACACTGCA TTGCCTGACT GATCACAGAG GTAGCTACAA 300
CCATGCAGGA ATTTGGAGAA GCAAGAGACA TCAGTGATGG GATTTCATAG CCATGGGACT 360
GGGGTACAAT CTCACCATGG CTTTTTACCT TGTTCATACA TATTTTTATG TGGAGCTGTG 420
GTTAGTTTCC ATTACCGTAT GGTATTTCAC TGCATGAATA TACCAGTTAT GTATCCATTT 480
CCTGTTGATG TCATTTGGGT TGTTTTCATT TGTTTTGGGG GAGGGGGTAT GTCTATTACG 540
AACAGTGCCA CTTTGGACAT TCTCATACAT ATATCCTGGG ACATGAGTAT GTGCATGAAT 600
TTCTCTAAGA TGTGTGTATA TATATATATA CACATATACA CACGTCTGCG TGGGTGTGTA 660
TGTAGGAGTG GAATTGCTGG GACACAGGTT TATTTTCAAC CTTACTAAAT AGATCAAAAT 720
ATTTTCTAAC ACGGTTGTAC TAACTCATAC TCCCACCAGG AGTGTAAGAG TTACTATTGT 780
ACTTGATATT GTCAGAGTTA TCTGGACCGG TACGTGTGTG ATGGTATCTC ACTAGGGTGT 840
AACTGGCATT TCCTTGATTA CTTGAGTGCC ATTTATTAGT GGCCATTTAG AGTTCTTCTT 900
TTGCTAAGGG CTATGCAGGT TTTACCCCTC TTCTATTAGG TCATCTTTTT ATTTCTAAAC 960
TTCCTTGAAG GTCTGTTCAA GTCATGGAAT CATAAAATTT TAAAACCTTG GCACTGGCAG 1020
GGACCTTAGA GAACTTCTGG TTCAGTATCC TCCTCAAGAG ATGAAATTGC AACTCATGGA 1080
AACGGACCTG CCTGTGACCC ACAGAGAATT ACTGCCTGCT GCAGGCTCAG AAGCCAGGTC 1140
CAAATCCAAA GCGTCTTCCT CCCTCCTCAT TTTCCTGCTG CCTGTCTGTC CTGCCAGCCA 1200
GTTACATGCA GCTGCCATCC ACCTGGTATT TCCTTCCCTC CTCACTGCAC TGCTGCAGCC 1260
CTCCTGGAGG AACCCATGCC AGCTTCTCTA ACCTGCACGT ATCAGGTCAC GTGCCTCCCG 1320
GGAGGGTGAG ATCCCGGGGC TTGGGCCTGT TATATTCCTG TCTCTAGAAG AAGGGCTGTG 1380
AGTGCAGGCC AGGAGGGGAA GCCGTGGCCC 1410
|
