| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41339 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:123742530-123744120 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr9:123743118-123743132 | 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 |
| GH09I120981 | chr9 | 123744061 | 123744190 |
|
Enhancer Sequence | TTCTGGAAAC AAGAGAAGAT ACTTCAGTTT CTATGTCAAG CAACCACCTA TCAATTGATA 60
TGAACTACCC TCAGATCCCA CTATCCTGGA GCAAGCAATA TGGGGGTGAA AAGAGGACTG 120
ACCTAATGGA AATGGATGGC TTCTCAGTGA AGCAAATCCC TCCGAGAGAA GGAGCAGAGC 180
ATAATCTTGG AAGGGACAAT GAGGTTGTCC AAATCAGGTT AAGCTTTTTG CCTCTGAATT 240
CTCACTTTCC TTTTAGAGGT TTTGTGCCTT TAGTTTCTGA GTACACCGTC AGACCTAGCC 300
TCCAGGAAGA AAAGGCACCG AGCATAGACA CAATTTCTTT TTTTTTCTTT TTTTTTGAGA 360
CGGAGTCTCG CTCTGTCGCC CAGGCTGGAG TGCAGTGCTG CGATCTCGGC TCACTGCAAG 420
CTCCGCCTCC CAGGTTCACG CCATTCTCCT GCCTCAGCCT CCGGAGTAGC TGGGACTACA 480
GGCGCCCCGC CACCACGCCC GGCTAATTTT TTTTTTTTGT ATTTTTGGTA GAGACGGGGT 540
TTCACCGTGT TCGCCAGGAT GGTCTCAATC TCCTGACCTT GTGATCCGCC CGCCTCGGCC 600
TCCCAAGTGC TGGGATTACA GGCGTGAGCC ACTGCACCCG GCCCATAGAC ACAACTTTTA 660
TTGTTCCCTC TCAGCGTAGT TGCAACAGGC ACACAGGTTC AAAAGGAGTT ACACTTAAAA 720
AAATAAATAA ATAAAACAAT AAGTAGCAGA AAGAAACCCT AACTGCCACA GTACTTTTAG 780
ATCCTAAGAA TGCCTGGGTA AATAGTCCCG ATCACTAGTC CTGACGCCAC CAAAATGGTT 840
GTGTTGGGCA AGTGGGCCAG CAGAAAGCCT GCTGCGATGC TGCTAACATC CTGCCTGCCT 900
CCTCTCCCAG CTCCACATGC ATCTCTCACC CATGTGGCCA CTAGGTGCCT GGGAACTAGT 960
CTTCATTGAT TATTTTGTCT TGTTAAGCTT CTGAAACAAA CTGAAAACAA ATGGTTTTGT 1020
TTTGTGCTTC CAGTTTTGCA AATCCACTTG AGATTTTCCA TCTCAACCTT GGAAATCTTC 1080
TATGTTGATT TACTTAGGTG GCTCATCACT TTTCTCCCGT TTCCAAGCAA ATGTTGTTTG 1140
GAAGGATTTG GAGGATACAC ATTTGCTGTT GTGTATCCTC AGTACTTGCA TGATACAGAA 1200
TGCTTTCACT ATAGGATAAC AGTAACATAT AAAGCAGGAT TTAGCAAAGA TAAGACAGAG 1260
AAGCTGGGGG CACTGGATCA TTCTTCCATC CCAGTCCCAG CTATCAGTTT TAGACCCAGC 1320
TCTACAATTT ATTAGCCTGT GACACTGGGA AACTGAATTC ACCTTACTTA GTCCTCAGCT 1380
TTCTCAACTG CCGATGAGTA GGTTGGACTA GGTGGTCTCT AATATCTATC ATTGTTCTGA 1440
AATCTTTCAA TTCTGGAGTT TAAGTTATTT TCAAGTTATT GGAAAGAAGG AAAAGAAGCT 1500
TTTGAAACAA AAGGTCTTCT GATTGGTGGC CCCTCCAGTA TATAGTACAG AAATAGATGA 1560
TGGGTGTGAG AGAAAGAAAA CTCTTACTTA 1590
|
