| Tag | Content |
|---|
EnhancerAtlas ID | HS108-14966 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:28093300-28094760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr16:28094549-28094562 | TTCTAGAAGCTTC | + | 6.28 | | Klf1 | MA0493.1 | chr16:28093978-28093989 | AGCCACACCCA | + | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr16:28093340-28093355 | GAGGTCAGGAGTTCA | + | 6.22 | | SREBF1 | MA0595.1 | chr16:28093512-28093522 | ATCACCCCAC | + | 6.02 | | Zfx | MA0146.2 | chr16:28093897-28093911 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH16I028082 | chr16 | 28094001 | 28094150 |
|
Enhancer Sequence | AATCCCAGCA CTTTGGAAGG CCAAGGTGGG CAGATCACTT GAGGTCAGGA GTTCAAGACC 60
AGCCTGGCCA ACATGGTGAA ACTCCGTCTC TACAAAAAAA ATACCAAAAT TAGCAAGGCA 120
TGGTGGAGCC CCACCCTGTA GTCTCAGCTA CTCAGGAGGC TGAGGCAGGA GAATCCCTTG 180
AACCCAGGAG GCAAAGGTTG CAGTGAGCGG AGATCACCCC ACTGCACTTT AGCCTGGGGG 240
ACAGAGCGAA ACTGTCTCAA AAAAATAAAT AAATCAAAAG AATCATATGT ATTGACACAT 300
GAAAATTATA TGAAATTGAA ATTTTGGTGT CCATAAATAA AGTTTTTGTT TTGTTTTGTT 360
TTGTTTTTTG AGACGCAGTC TGGTTGTGTC GCCCAGGCTG TAGTGCAGTG GCTCGATCTC 420
GGCTCACTGC AAGCTCTGCC TCCTGGGTTC ACGCCATTCT TCTGCCTCAG CCTACCGAGT 480
AGCTGGGACT ACAGGCACCT GCCACCACGC CCGGCTAATA TTTTGTATTT TTAATAGAGA 540
CGGAGTTTCG CCGTGTTAGC AAGGATGGTG GTCTCCATCT CCTGACCTCG TGATCCACCC 600
GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC ACCGCGCCCG GCCCATAAAT 660
AAGGTTTTAT CGGAACACAG CCACACCCAT TTGTTAGTGT TCTCCGTGGC TGCAGTTCAT 720
GCTCCGGTGG CAGAGTTGAG CATTCGAGAC AGAGACAACG GCCTGCAAAG CCTCAGATAT 780
TTTCTATCTG TCTCTTTTCA GAGAATGTTC GCTGCTGCCG GCTCTGCTAC ATTCCAGTCC 840
CTGCCTGGGT GTTGGCCACA CAGGGGTGGA TTAGTTTCCT AGGCCTGCCG AAACAGATTA 900
CCGTAAGCAC AGTGACTTAG AACAAGAGTT CATCTGCTCA CAGTTCTGAA GGCCTGAAGT 960
CAGAAACCAA GGGGCTGCCA GGGCCACCTC CCTCCGGAGG CTCCAGGCAA GAATCTGTCC 1020
CTGCGTCTCC CAGCTCTGGG GGCCAAGGGC ATCCCTCCTG GCGGCATCCT CCAGTCCCTG 1080
CCTCGCCTCC TCCTCGAGGT GCCTCTCCTC TGTGTGTCCC TTAGGACACT TGTCACAGGA 1140
TTTAGGGCCC AATGGATAGG ACACTTTTTC AAAATAAGGT CACATCCACA GGTTCTGGGA 1200
TGTGGATGTA TCTTTTGGGG CAGGGCACTC TGTAAAGTGG TTTCTTGCCT TCTAGAAGCT 1260
TCTTTTGTAA TCTTTTATTT ATTTTGAGAT TTATTTATTT TTGAGACAGG ATCTTGCTCT 1320
GTCACCCAGG CTGGAGTGCA GCAGTGCAAT CCTAGCTCTC TGCAGCCTCA AACTCCTGGG 1380
CTCAAGTGAT CCTCCCACCT CAGCCTCCCA GGGAGGTGGG ACTACAGTTA CACACCACCA 1440
CTTCCCGGCT AATTTTTAAT 1460
|
