| Tag | Content |
|---|
EnhancerAtlas ID | HS053-23261 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr2:225712570-225714220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr2:225713834-225713844 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr2:225713834-225713844 | GGCACGTGCC | - | 6.02 |
|
| | 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 |
| GH02I224848 | chr2 | 225713301 | 225713490 |
|
Enhancer Sequence | ATGTCCTGAA TGTTCTAATC CTGCCAATAT GCCACCTTAC CTGGTAAGTA GGACTTAGCA 60
GATGTGATTA AGTTAAGGAC CATGAAATGG GGAGATTATC CTGGATTTTC CAAATGAGCA 120
CAGTGTCATC ACAAAAGTCC TTATAAGAGG AAGGCAGAGT CATAAGAGAA ATGATACAGA 180
AGCCGAGGTC AGAGTGATGG GATTGTTGGG AAGGCTCAAA AGCCAAGAAA TGTGGGCAGC 240
CTCTGGAAGC TGGAAAAGGA GATGAACTGG AACCTTCCCT AGAACCTCCT GAAGGTTCGT 300
CACCCTGCTG CAAGCTCGAT TTTAGCCCTG TGAGTCATTT CAGACTTCGT ACCACCAAAA 360
CAGCAAGATA ACAATTGCAT ACTGTTTTAA GCTGCTAAAT GGTGATAATG TGTGAAAGCA 420
GCCATAGAAA ACGTCTACAA AAGCTGTGAT ATTGTGAATC TCAGGCATCC CATCAGCAGG 480
CTGCACTAGT CAGACCTTCA CTTTATGGTT AGAAATTAAA TTTTTTCACT GAAACTTCTT 540
TGTCTAAAGT TGTTTGTAAC GTAAGCTAAC ATGTATATAG TAATTGACCA TGAGCCCAAT 600
GACTTTCTAT GTGTTAGAGC AGAATGGTGA AGCTTCAGGC TGTGGAGTCA CATGGTCTGG 660
TTTGATTTCT CTCACTTATT ATGTGCCCTT GGTAAAGTTA CTTGACTTCT CTGAGCCACA 720
GTTTTCTCAT CCATCAAATA GGGAGGTAAT AATAGTGCCA ACTTCTTGGA ATTACTGTGG 780
GGATTAAGGG AGATGATGTG TGCATGGAAT TTAGCTTGAG GCTTGGCACA CAGCAGGAGT 840
CTTGGAAGTC TGCCAGGGCA AGGCTTGTTC CCTGTCATGT TTAGAGATGA CGGGATCCAA 900
GCTCCCTTAA GTTCAGGCAT GTTATAAGCC ATGGAATTGG CTCAGGCTCT AGTTCTCTGT 960
TCTCTTCCTT ATGACATGAA ATGCTGCCAT TCATTGGTAA AGCTATTTAA CACAATCTCT 1020
TCACTAGTCA GTGAAATAAA AGAAAAAAAA TTATTCACTG AAAAAGAAAA GAAGACAAGA 1080
TATATCCCAG CACTAAAAGC ATCTTTTTTT TAAATTTAAA TTTTAATTTT TTTAGTTGAG 1140
ATGGAGTCTT GCTCTGTTGC CAGGATGGAG TGCAGTGAGT GGCATGATCT CAGCTTACCA 1200
CAATCTCCGA CTCCCTGGTT CAAGCGAGTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAT 1260
TACAGGCACG TGCCACCACG CCCAGCTAAT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA 1320
CCATGTTGGC CAGGATGGTC TTGATCTCCT GACCTTGTGA TCCGCCTGCC TTGGCCTCCC 1380
AAAGTGCTGG GATTACAGGC GTGAGCCACT ATACCCGGCC AGCATTCCAT TTTTTTTAAA 1440
AGGTCACTCC TGTCCTGAAA TACATGAATT TGCAACGTAC TCCTGGAACA ACTGCCAATT 1500
AATATAGTTT AGAAATATTG GTAAGTACAT ACCTGCCAAG GCATGTCCTT AGTCTGATGA 1560
GGTCTAGAGA GAGTGTTTTT CACTGCACGG TTATCTGAAC ATTTACCCAC CTTTCTTAGG 1620
AACCGCTGGG GGCAGTGGAG GGCTAGCTCT 1650
|
