| Tag | Content |
|---|
EnhancerAtlas ID | HS052-14688 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr16:69564270-69565290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr16:69564751-69564765 | ATGACTCACTTCCT | - | 6.69 |
| | | 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 |
| GH16I069528 | chr16 | 69562797 | 69567422 |
| Enhancer Sequence | TCGCGCCACT GCACTCCAGC CTGGGCGACA GAGCAAGACT CCGTCTCAAA AAAAAAAAAA 60
ATATATTACT TCCCAGTCCT GTTTGTGGCA GACCTAGATG AAAGTTCTAG GAAACACATG 120
CTTTGGAATC AGCCTGAACT TGAATCTCAG GACCCAGTCT GTTCCTACCT GTGAGCCCTT 180
GGCCAAGTAT TTCTCCTCTC TCTGTCTCGT TTTCTCATCT GTGAAATGGG AATGCTAATA 240
ACACCTTTGC CGGATGAGTT GACATGAGAG TAAGAGGCGA GCTTGTGGGT GACCGCAGGC 300
AGTGCCATGA ATGACCCACT TTAGGTGCTG AGCACCCAGG AGCCCTTCTT AGTGCGATTT 360
GCCTGGGCTG CCTTGAGACC ACACATGTGA TGCGGGGGTG GGGGGGAAAG GGTAACAGAG 420
AGGAGCAGTG ACATGGAACA ATCCCAAGAA TGAAAGCAGG GCGGCGGGGC TGACTCACCG 480
GATGACTCAC TTCCTTGCCC AGGGATGTTC TGAGCATCCA CGGAGCTGCT TCTCATAGTT 540
CTCATACCCT TGGTTCCTTC TCTGTGGGGA AGGCAGGAGG AAGATGCCCC TCCTCGCCCA 600
GAGCAGGGAT CAGAATGTGG GACCTTCTCC GTCATACCCA GAACCATGGA GACTAGCTGG 660
CACCCCATTT TTTAATTCAC AAAATAACAG TCCCCATAAG ATGTAATCTT TTTAAGGAAG 720
AATAGTTTTT GCCCCAGGAG TACAGGAGAG ATTCTAGACT CCTTTTGCCC TTTTCCAAAT 780
TATCACAGGG AGATCTGGAC CCCGTAGAAT ATTTGAAAGT GCAGAAAAAT GCAAAGAAGC 840
AGAAAAAATC ACCTATAATC CTATCGTTTA AACTTTATCA CAGTGATGAG TTTGGTATTT 900
TTCCATTCTA TTTTTTTTCT CTGTATTTTT TCATTATATA GTCAAGTTTC TGCAGTCTAT 960
ATCAGCACTA TTCAAAGGAA ATATGCAAAC CACAGGTGTG AACCATATAT GTAATTTAAA 1020
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