| Tag | Content |
|---|
EnhancerAtlas ID | HS108-08560 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:113060670-113062060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr11:113061285-113061299 | TGATGACGTGGCAT | - | 7.82 | | ZNF263 | MA0528.1 | chr11:113061432-113061453 | TTCTTCTGCTCTACCTCCTTC | - | 6.2 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_36945 | chr11:113044372-113066246 | HSMMtube |
|
| | 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 |
| GH11I113187 | chr11 | 113058210 | 113065350 |
|
Enhancer Sequence | GTTCTTTTTG GATGTAGCAT TATTCTGGGC AGGAAGACAG GAGCATAATT AGCACATGGG 60
GGAGGTCCCA GTGACCAAGT TTGTGTGTTT GGTCGTGTTC CCCCAACCTC ACTACTCCTA 120
CCAGTGAACC ATTTCCCCAG CCCTCCCAAC TGACTCCACC TAAATCTTTG ATTTATTATA 180
AGTCAGAAAA AATGGATAGC AACCTTGAGA GCAGCCAGAG GCCCTTGCTG TTCTTAGACA 240
CATAAATCAC AAGGTAGAAG TACGAAGAAT GAAGACAGAA TGTCAGTAAC CAGCCTGGGG 300
GTTGGGGAAG GATTTTGGGA CTTTTCTGGA TCTCTGAAAT TACAGCGTGT GAAGACAGGA 360
GGAGGCCATC CACATAGCCT GAGGACTGTT AACTAACTGA GAAGGAGAAA GTAATGCTAT 420
GGGTAATTCT GTGGATGGAT GCATCATAAT GTTGCCAGAT GTAATACTGC AGACTCACAG 480
AAGAAGAATG TATTTTGGAT GTGCCAGCAC CGCCCCACGG CCACCATCTG CTGCTGCCCC 540
TTCTCCTCTC CCCTCTCCAC ACCCAGCCCT AGGTTGGGCT ACTCTGGGTT CTGAGTTCCT 600
GATAAGCCAT GGTCATGATG ACGTGGCATT TCCTACCCTG ATGAGTGGTG AAAAGCTGTG 660
GGTTCCAGGG ACAGCTTCTC ATTTGTTCCC TAACTCAAGA AAGCGAAACA ACGATGTCCC 720
AGGGTATTCT GTTTGGCAAG TTATTATTCA AATGGCTGGA TTTTCTTCTG CTCTACCTCC 780
TTCAAAATTT TGTATAACTT AGTTTATGTA TTATCTAGCA GGTCAGGCAC CATCTGATCT 840
GGTGTGACAG TGGTTGTGGG GGTGGGGAAT GGACTCTCCA TCCAGTAGAA GAGTGTGACC 900
TCCAACAGGA ATCCCTTTAA CATGGACACT CTACAGATGA CCCCTTAAGG AGAATGGCTG 960
CTTGGAGACA GCACAAGTTG AGTGGCTATA TGAATAATCT GTTTCAAATG CACACTCTGC 1020
AGGGAGTGGG GGCAGAACCA GTCACAATTT ATGGATCATC AAAGGATAAT TTTATTATCA 1080
ACGTTTTAAT AAGGAAAGGT ATGGCTTATC CAGAACCCAA ATTGGGGGAT CAGTAGTAAT 1140
CCATAGATGG GAAAATGAAA ATCCAACTAG CAGCCCCCGA CCCCATCCCT GTTGGCATCC 1200
ACCACCAATG CTGAGAACTG AGCTATAGAG ACAGAAGGGA AGGGCTGCAG GTGGACATTG 1260
AGGCTGGACC CACTGGTGGT GAGGAGCAGG GTTGGAGGGA ATTCGGTTCA GAGAGGAAGG 1320
AAAGTCTACG GCAGGGAGAA GAGTGTAGCC AGGTGGGCTC AGGAATTCCA GCAACCTGTT 1380
TCCATTCCCT 1390
|
