| Tag | Content |
|---|
EnhancerAtlas ID | HS092-14566 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:45941060-45942080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr13:45941085-45941097 | AAACAAACAAAC | - | 6.32 | | HES2 | MA0616.2 | chr13:45941300-45941310 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr13:45941300-45941310 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr13:45941218-45941233 | GAGGTCAAGAGTTCG | + | 6.24 |
|
| | 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 |
| GH13I045366 | chr13 | 45940916 | 45943622 |
|
Enhancer Sequence | AGCAAGACTC TGCCTCAAAA TAAATAAACA AACAAACAAA AATATCTGGC AGCAATTTTC 60
AAGCATTCAA AAGAGATGTG AAGGAAAAAA ATTTGGCCGG GAGCAGTGGC TCACGCCTGT 120
AATCCCAGCA CTCTGGGAGG CCAAGGTGTG CGGATCACGA GGTCAAGAGT TCGAGACCAG 180
CCTGACCAAC ATGGTCAAAC CTGGTCTCTA CTAAAAATAC AAAAATTAGC TGGGCATGGT 240
GGCACGTGCC TGTAATCCCA GCTACTCAGG AGTCTGAGGC AGGAGAATCG CTTGAACCTG 300
GGAGGCAGAG GTTTCAGGGA GCCGAGATCA CACCACTGCA CTCCAGCCTG GGCAACAGAG 360
GGAGACTGTC TCAAAAAAAA AAAAAAATAA ATAAATCAGC ATAGTAATTG ATGAGGACAA 420
GGACATTTTA TTATCATGGG ATTATGGGGA CAAATGATTG CTGAAATCAT AATTAGCTTT 480
CTGGCGGGGG AAGATAGTAA GGTAGAAAGA GGAGAAATGG GTGTAATCAA AGGAAGTGGC 540
AGAGAGAGAT TAAAAAAAAA AAACAGGAAA TGAGAACAAG AATATGACTA ACAATGCCTG 600
AGCCCCACCC ACCCATCCTC AGAGTGGACT CCCTCTCTCA AAGGCTTGTG GGCACCTGCC 660
CCCGAGCTGA CTCACCCTGT TCAGTCATCA CAGCTCACTG CAGTGATGAA GGCTCAGGTG 720
ATCCTTTCAC ATCAGCCTCT CCAGTAGCTG GGACTAAAGG CATGTGCCAC CATACCTGGC 780
TAATTTTTTG TTTTTGTTTT TGTTTTGAGA TGGAGTCTTG CTCTGTCACC CAGGCTGCAG 840
TGCAGTGGCA TGATCTAGGC TCACTGCAAC CTCCACCACC TGGATTCAAG CAATTCTCTG 900
CCTCAGCTTC CTGAGTAGCT GGGACTACAG GTGCCTGCCA TGACGCCCAG CTAATTTTTT 960
TGTGTATTTA GTAGAGATGG GGTTTCACCA TGTTAGCCAG GATGGTCTCG ATCTCCTGAT 1020
|
