| Tag | Content |
|---|
EnhancerAtlas ID | HS108-08718 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:119995100-119996260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr11:119995795-119995808 | CAGTTGACCTCTG | - | 6.15 | | ZNF263 | MA0528.1 | chr11:119995549-119995570 | CTCACCCCCTTCTCCTCCCCC | - | 6.95 | | ZNF263 | MA0528.1 | chr11:119995546-119995567 | CCCCTCACCCCCTTCTCCTCC | - | 7.36 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26582 | chr11:119985447-119997137 | Esophagus | | SE_36164 | chr11:119990825-119996181 | HMEC | | SE_57595 | chr11:119994776-119995560 | VACO_503 | | SE_64461 | chr11:119991394-119996028 | NHEK |
|
| | 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 |
| GH11I120119 | chr11 | 119990523 | 119996803 |
|
Enhancer Sequence | ACCGCCAGCC GCAGCTTCTC AGATGAGAGG GCATGGGAGA CTGAACAGCA GAGTGTTCAA 60
CCCCGCCGTA CCCCCTACCG AGCAGTGCGC CCTTTGAAAG GATGCTTCTC TGAGCCTCAG 120
CCTTCTCGCC TGTAAAATGC AGTACACCCC ACAGGGAAAA TAAGGTAATG TGCGTGAGAA 180
GCTCAGTGAA ATGCCCGGCA TCGAGCGAGC ACTCAATCAT TGTCAGCTGT CACCATCACC 240
ATTAGCATCA TCACTATTGT CATTAGAAGG AGGATTTCGG GATCTGAGTG CCGTTTGAAG 300
CCAAATGATT GTCTTGCTGA AATGGCTTAT CTGTCCTTGT GTGTGATTGA ATGTCCCCCA 360
CATTTCACAG GGACACCATG TGATATTGCC ATCGCCAAGG TGCACAAATG GCCTCCTGAA 420
CCCCAACCCT TCTGCACACT TTTATCCCCC TCACCCCCTT CTCCTCCCCC AAAGAATCAT 480
ATGCTGTGTC TGGAGAGCAA TCAGGGGTCC TTTCCTTTGG GGTATTCACG TCTAGCAGTC 540
ATTAACAAGG CTGTACTCTC AAGGCCCCGT GCAACGCCTG GGACACCGGG TGGGGCCTTG 600
GGGAAAGTGC CCAGGCTTCA GGCCCTAAAG GGACTGGGTG GAAAAGGACT TGACGATGTT 660
GTTTCTCAGG TTCAGAGGTT TTCTGTGAGA TGATTCAGTT GACCTCTGAG GGGACAGCAT 720
GACTCAGAAG AAGAGCTGAC TTCAAGGGAG CTGGTGAGTC ACAGAGACAC TGTGTCCCAC 780
CGTCCCCAGC CCAGCTCAAC AGGCCAAGTC CAGCCTCTGG GCTCAGCACT GCTCAGCATG 840
GCCATGATGA CAGGCAAGTC CTCCCTCCAG GCATGGCTGC AGTTCTAGGT CACGTCTGCT 900
AGAGTCTGCA AAGCCACCAG TTTGGAATCT GGCCCATACT AGTGGCAGCA TCCACACAGC 960
TGCTGGGCTG GGCCCGGCAA TTAGATGTAG ATCTGAACGA AACCAGTCTC TGAGTTTGAT 1020
GGACAACCCA CAGAGAGGAG GCATTTGTGG AGCCAGTGCC CAGGATGTCC CTGCTCTGGA 1080
GGTCTCTTCC TATAGTTGCA TAACTTTGGC AGCAAGTTCA AAGGAGGAGG AGGGTTAGAA 1140
TCCCTGTATC CTAGTCCAAA 1160
|
