| Tag | Content |
|---|
EnhancerAtlas ID | HS052-11039 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr13:114605990-114607210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PHOX2A | MA0713.1 | chr13:114607159-114607170 | TAATTGAATTA | - | 6.14 | | Phox2b | MA0681.1 | chr13:114607159-114607170 | TAATTGAATTA | - | 6.14 | | RFX2 | MA0600.2 | chr13:114606055-114606071 | GGTTTCTATGGCTACC | + | 6.18 | | RFX2 | MA0600.2 | chr13:114606055-114606071 | GGTTTCTATGGCTACC | - | 6.27 | | ZIC3 | MA0697.1 | chr13:114606809-114606824 | GACCCCTCGCTGCGC | + | 6.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I113904 | chr13 | 114607081 | 114608387 | | GH13I113903 | chr13 | 114605981 | 114606944 |
|
Enhancer Sequence | TTTTCCCATC ATGCGTGTAT TACAATGGAA ACTTCCAACG GGACGCCGGC CCCACCCTGT 60
GTGCTGGTTT CTATGGCTAC CTGTCATGTC CTCCGCACCC TCTCCTCTCC CCTGAATACA 120
GTTCCTAGAG ACCTTGAGTC CACAGCCCTG GGGCTCTGCA CACTGCGGGT CCGGTGGTGT 180
TTCCAGCGCC GTGTGGATGA CTTCCCCGCG TGTTTCCCCC TCTACACAGT TGAGGAACAG 240
AGAAGATCTC CACTTGCCAA CGGACACAGC GCTAGTGAAG CCAATTATTG CTACATCCAC 300
TGATAAAGTT CGGGGGGAAT TAAATTTTTT GGTCCATGGA TGCAAATCGC CTCCAGGCAC 360
CTTTACTATC TCAGTGCTCT CCTCAGGAGG CTGCTGTTGG TGGCCAGGGA TTTTGCCATA 420
GCAAAGTTCT TACAGATTCC CAAACAATAG CACTCAGCTG TCTGCCTCTC TGGCAGGAGG 480
ACGGACATTC GCAGCTTTGG ACTCATTTTC TTCCAAATAT GAACACTTTC AAAGACAGGG 540
ATCTGCCAAT GACTTTACCA GGAGGGCCTT GCCGGAGCTG TCACTGCTGT GGCATGCAAG 600
AAAGCAAGAG TCCTCCAGGA AGCCGGCCAA GAGGCGCCTT CTCTTAGGCC AAACATGGGC 660
AACATGAGAA TAAGAATACA CAAAATCAGG AGAACTAACA GGAGGCTGTG AGGAACTCAC 720
CCCAAATAAT GAGGAAGCTG GAGAATAAGA CCAGCCTGGT CCAACTAATG GCTGCTCCGT 780
TGGAGGCACA GGAGTGCAGA GGCAGCGAGG CCTGCAGAAG ACCCCTCGCT GCGCTGGGCG 840
GCAACTCCAG TGAAAAGCTG CTAATCAAAC ACAACTGAAT TCACACTATT TTAAAAATAA 900
GTCTGTAAAG GCAAAACAGG TTAATAGTAT TTTGACACTA AGCTTGTAGT TATAACAGAT 960
ACTTTAAAAG GTCAATCCCA GTTACCACGG TGACTGCAGC TCAGGCACCG CAGAAGTGCG 1020
TGAGGATGAG AGTGAGGGAG CCGCAGCCTG GAAGGGTGGG TCCCAAAGTC TCACTGGCTG 1080
ATAGGGTTTG GCTGTGTCCC CACCCAAATC TCACCTTGAA TTGTAGGTTC CATAATCCCC 1140
ACGTGTTGTG GGAGGGACCT GGTGGGAGGT AATTGAATTA TAGGGGCGGG TTTCTCCCGT 1200
GCTGTTGTTG TGATAGTGAA 1220
|
