| Tag | Content |
|---|
EnhancerAtlas ID | HS111-02995 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr2:131148380-131149600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr2:131148899-131148909 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr2:131148904-131148914 | GGGGCGGGGC | - | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24626 | chr2:131147719-131149510 | Colon_Crypt_2 | | SE_54336 | chr2:131147147-131150225 | Spleen | | SE_59968 | chr2:131142050-131151696 | Ly4 |
|
| | 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 |
| GH02I130389 | chr2 | 131147366 | 131150173 |
|
Enhancer Sequence | CTACACAGAC CTGCGGGGGT TTAGGGCTGC AGCCAATGCG CCCTGGCTGG GGTCTCCCTT 60
CGGACCCACA CCCACCCTGG CCACCTGCCT GAAACCCAGG AGGTTGGCTG GGGAACCTCC 120
AGGGTGTACA GTTACACGCT GTACTCTGGG GTGGCGGACA GGGGGTCACT TGCACTCTGT 180
CCCCAGGGTA CCCGTGCAGT CCCTGCCCTT CCGGCCCGCG GTGGGAGTGT GCTGCAGCCT 240
CGGGCGCTGA TCTGCAGCCT GTCACCTGCG CCAACGCCCC TTAACGCCCT TCTTCTCATC 300
CCCATTTTCC GGTGCCCACC AGTCCCCTCG TGCTGACAGA CGACTCAGCG TGTCTCCCCA 360
GAGCTGCTCT GCGAACTGCA CCCGTGGAGG AGCCCATACT TTCTGAACAG CCGCTTTGAT 420
CTACTTAAGC ACTGCCGTGT TTTCATAGCT ATGGCCCAGC TATATCATAG GACATATATC 480
CTATGTCATA GCATAGCGGT GACAGCAGCA GGCGGCGTTG GGGCGGGGCG GGGCCAGAGT 540
GACAGGCAGC CCTGCGGGCC CCTGGCCCCT CCCCACAGCC CCTGAGACTT GTGCGGCCCG 600
CAGGAATCTT CTGGCGGCCA CCCGGTTCGC CGGCAGCACT GTATCAGTTT CTACATGGCT 660
CCTCTCCCAG CCCCTTACGT GGCTTATTTC GTGTCAATTC TAGGGAGGTT CTACCGTTTC 720
CGTTCGCCGG GGGTCTGGAA CGCGCACGGG CCCTGGGCGA GCCTCCCTGA GCGCCGCCAC 780
GTCCGCCTTC GTCGTCCTCC CAACCGGACC CCGCACCCCC GCCCTCCCTA GCGCTGTGCT 840
GGACGCTTCT CTGTGAGGAG AGTCCCTCGC CCCTTCTTCA GATTTGGGAA TGGACTCTCG 900
GGCACCTGAA GCGCCTGCTC AGGATCAGGC CGGCACCTGG ACATGAATCC CAAACAGAAA 960
GCCTGAGCCC TGCCTGGCGC TTTCGCGGCT GCTGGCACGG CTGCGCAGAA ACGCCAGCGT 1020
CCCTGGACCG AGCGCGGGGA GGGGCAGGCT TCCAGCAGCG CTGTCCACTG GGAAGAAGAC 1080
ACAACCCACA TTTTTAGATT TTCCAGTTTC CACGTTGAAA AAGCAAAAAG ACATGAGATT 1140
GATTTGTGAC CCAGTGTATC AAAAATATTA TTTAACCGAT TAATCAATAT GAACAATTGT 1200
TCATTAGATA TTTTACTTGT 1220
|
