| Tag | Content |
|---|
EnhancerAtlas ID | HS108-17506 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:60710820-60712180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr17:60712033-60712050 | AAGGTCTTTGTGACCTG | - | 6.09 | | ESR2 | MA0258.2 | chr17:60712034-60712049 | AGGTCTTTGTGACCT | - | 6.63 | | Nr2f6(var.2) | MA0728.1 | chr17:60711880-60711895 | TGAACTCCTGACCTC | - | 6.22 | | STAT1 | MA0137.3 | chr17:60711479-60711490 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr17:60711479-60711490 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr17:60711479-60711493 | TTTCTGGGAAAGGG | + | 6.56 |
|
| | 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 |
| GH17I062632 | chr17 | 60709817 | 60712148 |
|
Enhancer Sequence | GCCACTGCAC TGCAGCCTGG GCAACAGAGC GGGACTCCGT CTCAAAAAAA AAAAAAAAAA 60
AAAGAGAAAA CATGACTATC AAGGTTCCCA AATATGATAA AACACAGTCT TCAATATACA 120
AAATCCTGCT GGACACGGTG GCCCATGCCT GTAATCCTGG CTTGAGCCCA GGAGTTCAAG 180
ACCAACTTGG GCAACATGAC GAAACCCAGT CACTACAGAA AAAAAAAAAA AAAAAGCTGG 240
GTGTCCTGGC TCATTCCTGT AGTCCCAGCT ACTGGGCAGG CTGAGATGGG AGGATTGCTT 300
GAGCACAGGA GGTTGAGGCT GTAGTGAGCC ACGATTGCAT CATTGCATTC CAGCCTGAGT 360
GACAGAGTGA GACCCTGTCT CAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA 420
AAATCCTAAC TACAGCTGTC ACCAGAAAGG AGGTCCAATC CAGACCCCAA GAGAGGGAAC 480
TCACGCAAGA AAGAATTTGA GGCGAATCCA TAGGGAATAG TGAAAGCAGG CTTAATAGGA 540
AAGTAAAGGA ATAAAGAATG GCTACTCCAT AGGCAGAGGA GTAGCACTGA CGGCTCAGCT 600
GCTTATACAA TTGTTACTTC TTGATGATAT GCTAAACAAG GGGTGGATTA TTCATGAGTT 660
TTCTGGGAAA GGGGTGGGCA ATTCCCGGAA CTGAGGGAGT CTTCCCTTTT TAGACCCTAT 720
AAGGTAATTT CTTGACGTTG CCATGACATT TGTAAACTGT CGTGGCGCTG ATAGGAGTAT 780
CTTTTAGCAT GCCAATGCGT TATAATTAGT GTATAAAAAA ATGGGCAGTG AGAATGACCA 840
CAAGTCATTT TTTTTTTTTG AGATGGAGTC TCACTCTGTT GCCCAGGCTG AAGTGCGATG 900
GCGTGGTCTT GGCTCACTGC AACCTCTGCC TCCCAGGTTC AAGCAATTCT CCTGCCTCAG 960
CCTCCCAAGT AGCTGGGACT GTAGGCATGT GCCACTACAC GTGGCTAATG TTTGTACTTT 1020
TAGTAGAGAT GGGATTTTAC CATGTTGACC AGGCTGGTCT TGAACTCCTG ACCTCATGAT 1080
CTGCCTGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA CGCCTAGCCC 1140
AGAGATCACT TTTGTCACCT TTTAGTTTTG GTGGGATTTG GGTGGCTTCT ATACTGCGTG 1200
CTGTTTTTTC AGCAAGGTCT TTGTGACCTG TGTCTTGTGT TGACCTCCGG TGTCATCCTG 1260
TGGCTTAGAA TGCCTAACCT CTTGGGAACG CAGCCCAGGA GTTCCCAGCC TCGTTTTACC 1320
CAGCCCCTTT TAAAGATGGA GTTGCTCTGG TTTGAACACC 1360
|
