| Tag | Content |
|---|
EnhancerAtlas ID | HS108-08640 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:117931200-117932480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr11:117931768-117931779 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr11:117931768-117931779 | CTGAGTCACCC | - | 6.02 | | Myod1 | MA0499.1 | chr11:117931268-117931281 | AGGGACAGCTGCC | - | 6.48 | | NFE2L1 | MA0089.2 | chr11:117931764-117931779 | TCTGCTGAGTCACCC | - | 6.63 | | Nfe2l2 | MA0150.2 | chr11:117931766-117931781 | TGCTGAGTCACCCAT | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 117931733 | 117932023 | | chr11 | 117931677 | 117931995 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I118060 | chr11 | 117931677 | 117931995 |
|
Enhancer Sequence | TTCCCAGGCC GGCAGCGAGG GCAGGACAGG GGCCAGGCAG CCCTGGGAAG CCTTAGTGGT 60
GGAAACCCAG GGACAGCTGC CATGCTCACC TGGGAGACTG TCCTTGGCCG CCTTTCTTCT 120
AGGCTTAGCA TCCTGTGTTC CTCTGGACCC CCGGGGGTCT GGGAGAGCAA CTGCAAATGG 180
CTGTCTGGGA CCCCCTTCTA CAGAGTCCAG GGTGTCCCTC TGGCTGTTCC CCTCGCCACC 240
CCTTCCTCTA ATTCCCTGCC AGCTCCAGGT TCCCTGGAAT GCTGGTTCTA ATCTGGCTTC 300
CAAGTCTCTC TTACCAGCCA GACATGGGTA CTCCCATCAT CCCTCCCACA TGGCTGCCCT 360
CATCCTTTGG ATCCCCAGGC AGACACCCAC CCTGGCCCCC TTTTAATTTT CCTTTTTTGA 420
TCTATAAGTA AGAGAGGGAC AGAGAAAGCA CTTCCAGGCT GCCCCTCTCC AGCCCTGTGA 480
CCTCACATCA CAGTGTCCTG GTTGCAGGTT GAGGAACTCC AGTGGGAGGC GTCCAGGCCA 540
GCAGAGGCTC CCAGAGGCAC CGCTTCTGCT GAGTCACCCA TTCTAGCATA TGGTCGTGGC 600
CCTGCTTGTT CCAAAACGGG ACACCTTGCA CTGCCACTCG TGACAGACAC ATGACACCCA 660
CAGTGGGAGT GATTGAGAGG CTATAGACAG GCCAAGGCGC AAGCCCAGCA TCATTTTCAA 720
CCCCGCCTCT TCCAAGAAGG GAGGTGATTA AGACTCCAAG CTTCAGCTGC AGAGAGACCC 780
AGCTTCAAAC CCCAGTTCTG AGAGTGTTTC CCTGTAGGTG AAATGGAGAA AATAATGCCC 840
ACCTCACAAG ATTGAAAAGA TTGGATGATC GATTCACAGA AGGCATTTAG CAAGTTCTCC 900
CTCAATAAGT GGCATTTCTA GCTACTTTTA TGCCAATGTA TTACATTTTT TAAGTAGTAA 960
ATTATTTCAG GGACTAGAGT GGCAGGTCCC CAGCTGGAGC TACCTTCTTC TTGGCATTAG 1020
TGCTCCAGGG AAGCAGAATC AGTAACTAAG TTACCAGACG AACACCGTCG GATCAAAGGA 1080
AGTGGGAGGG GTGGGGGATA CTTCACCTGA GCCCTGGGAA AACCTCACAG ATCCTGCTGG 1140
CCTCCACAGA GGCAACCTCT GTTAAGCAGA ACCTGCTTAT GTTCCCCACA GCCCTTCCTG 1200
CGACCTGGGC TGCTGGACAC CGATTAGCTT GGATCTACGG GGCCCATTTC CTCTGCACCC 1260
AGGACCGCTC TTTGGTGACT 1280
|
