| Tag | Content |
|---|
EnhancerAtlas ID | HS108-07191 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:33228810-33230200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr11:33229397-33229409 | GGGCACGTGGGG | - | 6.07 | | STAT3 | MA0144.2 | chr11:33228903-33228914 | CTTCCCAGAAA | - | 6.02 | | Tcf12 | MA0521.1 | chr11:33229348-33229359 | CAGCAGCTGTT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 33228968 | 33229530 | | chr11 | 33229831 | 33230073 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I033207 | chr11 | 33229147 | 33229346 |
|
Enhancer Sequence | CGTGAGCCAC CACTCCCGGC TGAGAACCAC AGTTTTAATG AAAATGTTAT TGTTATGTAT 60
GTTTTTATTA TATCAGGGCA AGTGCACTCA AAACTTCCCA GAAATTATTT AAGTCTCTAC 120
AATAATCGTT TTACACTGTT TATCACCATT TTATAAATGA GGAAACAGGA TCAGAGAGAT 180
GAAGTCATTT GTCCCAGGTC ACACAGTGAG TAAGTGACTG ATGTGAACAG CTCCAGCTCT 240
TGGCCTTACC TCACCCAGCT CACTATATCC CTTAGCTGGG AGTGCATTGG AAAACTATGG 300
GTCTCTGGCT CAGGGCCCAG CAGTGAAATT GCTGGAACTT CAACCCCCAC CCTTCCCTCC 360
ATCTCCTGGA AATGTCTGTG TTCTGGTTCC AGGAACTGCT GAGCCACCTT GCTGGTGGTG 420
GTTGCCTCTC CTCTGCCCCA GCCATCCGTC CTCCCTGCCT CATTTCCATG GTCACGATTG 480
CTCTTAAGGA AAGCGGGGGA GCCTCTGCTT CCAGTTTCCT GCAGGGCTTC AAAGAAGGCA 540
GCAGCTGTTT TATTTGATTT GGTTTTTATT CCAGGGGGGC CTGACATGGG CACGTGGGGC 600
TGGCCTGGAA GGCTGTGTCA CCTCTTACTT AACAGTGCCC CTCCCATATC CCAACTAAGC 660
TAGCATGCTC AGCTTCTCTT TCCTTTCCAA GTGAATTCCT GCTCCAACTG TTGACTTGTA 720
TGAAAACTTA AAAGGGGCAC CATTATTTAC CAGGTCCTTA GGTGAATTTC AGCTCTGGTG 780
GCCTGAAACT AGCCTCATGC TTCTCAAACG GGAGTCAGCC AGTCACTTAA CAGTCATATC 840
CCTCGAAATA GGCAGCGGTG TCATGGAAAA GTAATAGAGG GTATCTTCTG GGACTCTCAA 900
TTTTTCTGAA TGGTGCCTGA TTTAAAATAT CTTAATTTCA TGACAAATAT GGCAGCATAG 960
AATAGAAAAT GTTCATGAAT GTTTAGGATA AACCCTGTGA TTTAGATTCC TAGCTCTTGG 1020
ATGTTCTGTA GCCTATTCTA CCTCCTTCTC CTTCCCACCT CCATCTTACC GTCAGACCAT 1080
CAGAGCTATA CATGTCTTAG AGGTAAAAGC TGGAACTGCA TTGGCTGAAG ATATCTTCTA 1140
TATGGTTATT AGGTTTTTAT GGTAATAATC CACTAATTTT CCCCAAGTCC TCCATCCCCA 1200
CCCCAAACAT GTGCATTCTC AAAAGATGCT TTGCTTTGTC ACTCACTGTA GGGTGCCTTT 1260
GTATGTACCC TGTGGCAGAG TCTGTCTCTT TTTTTTTTTT TTTTTTTTTG AGACAGAGTC 1320
TCACTCTGTC ACCCAAGCTA GAGTGCAGCT GCATGATCTC AGCTTGCTGC AAACTCTGCC 1380
TCCCAGATTC 1390
|
