| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00760 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:23865840-23867110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:23866477-23866496 | GGCTGCCACCTAGAGGTGA | - | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr1:23865976-23865991 | GAGGTCAAGAGTTCG | + | 6.24 | | ZBTB18 | MA0698.1 | chr1:23866634-23866647 | TTTCCAGATGTTT | + | 6.28 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09947 | chr1:23865865-23866650 | CD14 | | SE_23782 | chr1:23866175-23866507 | Colon_Crypt_2 | | SE_34689 | chr1:23865879-23867213 | HeLa |
|
| | 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 |
| GH01I023539 | chr1 | 23865911 | 23867050 |
|
Enhancer Sequence | CCAAGATCGT GCTACTGCAC TCCAGCCTGG GCGAGAGTGA GACTTTGCCT CGGAAAAAAA 60
AAAGGCCAGG CACAGTGGCT CAATCCCAGC ACCTGTAATC CCAGCACCTT GGAAGGCTGA 120
GGTGGGTGGA TCACTTGAGG TCAAGAGTTC GAGACCAGCC TGGCCAACAT GGTGAAACCA 180
TGTCTCTACT AAAAATACAA TAATTAGCCA GGCATGGTAG CGCATGCCTG TAATCCCAGC 240
TACTTGGGAG GCTGAGGCAG GAGAATTGTA TGAACCCGGG AGGTAGAGGC TGCAGTGAGC 300
CGAGATCACG CCACTGCACT CCAGCCTGGG TGACAGAGCA AGACTCTGTC TCAGGAAAAA 360
AAAAAAGTAG ATTAGTGATT GCTGGGAATG GGTCAGTCTC TGTACAGATG AAGAACATGA 420
GGCTCAGAGA AGCCAATTGC CACCCATCTG TGTGACTTTG GACCAGTGAC TTCACGTCTC 480
TCAGTTGTGA CGTGGAGAGA ATGACGTGCG CCTGAGATGG TGGCTCTGCA GCTCAGTAAA 540
TGTGCCTGCG GCGCCTGGTG GGTCCCCCTG CGTCTTCGTT AGTTCCTTTT CCTTCTCTCA 600
GACCTTTGGC TGGAAGCTGG TGGGGCTGAA AGGTGAAGGC TGCCACCTAG AGGTGAACTC 660
TGGCACCTGC CAAAGCCTGC GAGGCGTCTT ATCTTCTCAT CAAGGTAACT CACCCGCTAT 720
GGGCTTGGGG AGGAGAAACA GGATGTGAAA GAAGCAGCCC CGCTGAGGAC AGGGCTACTA 780
GACTGGCCAG ATTCTTTCCA GATGTTTGTA GGCCCTGGGA ATGCTTTTCA CAGATGTTGG 840
GTCCCGTGGA GGTGATCCCA TGCGGGAAGA GGGACATCCA TGCGGGAGTC AGGTCCCAGC 900
AGAGCTGCTT AGCGTCTCTT GGGGAAATGC CACCTATAAT TCCTTCTTCT TCTTTTTTTT 960
TTTTTTTTTT TGAGATGGAG TCTCGTTCTG TCGCCCAGGC TGGAGTCCCG TGGCGCGATC 1020
TCGGCTCACT GCAAGCTCCG CCTCCCGGGT TCACGCCATT CTCCTGCCTC AGCCTCCCGT 1080
GTAGCTGGGA CTACAGGCGC CCGCCACCAC ACCCGGCTAA TTTCTTTTGC ATTTTTAGTA 1140
GAGACGGGGT TTCACCATGT TAGCCAGGAT GGTCTCGATC TCCTGACCTC GTGATCCGCC 1200
CCTATAATTC CTGTAATTGT CAGTTTATTC CCTCGTTTTC CTGAGGGATC TCTTTAACAC 1260
ACACACCTGA 1270
|
