| Tag | Content |
|---|
EnhancerAtlas ID | HS098-31477 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:131148520-131149870 |
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 | GTACTCTGGG GTGGCGGACA GGGGGTCACT TGCACTCTGT CCCCAGGGTA CCCGTGCAGT 60
CCCTGCCCTT CCGGCCCGCG GTGGGAGTGT GCTGCAGCCT CGGGCGCTGA TCTGCAGCCT 120
GTCACCTGCG CCAACGCCCC TTAACGCCCT TCTTCTCATC CCCATTTTCC GGTGCCCACC 180
AGTCCCCTCG TGCTGACAGA CGACTCAGCG TGTCTCCCCA GAGCTGCTCT GCGAACTGCA 240
CCCGTGGAGG AGCCCATACT TTCTGAACAG CCGCTTTGAT CTACTTAAGC ACTGCCGTGT 300
TTTCATAGCT ATGGCCCAGC TATATCATAG GACATATATC CTATGTCATA GCATAGCGGT 360
GACAGCAGCA GGCGGCGTTG GGGCGGGGCG GGGCCAGAGT GACAGGCAGC CCTGCGGGCC 420
CCTGGCCCCT CCCCACAGCC CCTGAGACTT GTGCGGCCCG CAGGAATCTT CTGGCGGCCA 480
CCCGGTTCGC CGGCAGCACT GTATCAGTTT CTACATGGCT CCTCTCCCAG CCCCTTACGT 540
GGCTTATTTC GTGTCAATTC TAGGGAGGTT CTACCGTTTC CGTTCGCCGG GGGTCTGGAA 600
CGCGCACGGG CCCTGGGCGA GCCTCCCTGA GCGCCGCCAC GTCCGCCTTC GTCGTCCTCC 660
CAACCGGACC CCGCACCCCC GCCCTCCCTA GCGCTGTGCT GGACGCTTCT CTGTGAGGAG 720
AGTCCCTCGC CCCTTCTTCA GATTTGGGAA TGGACTCTCG GGCACCTGAA GCGCCTGCTC 780
AGGATCAGGC CGGCACCTGG ACATGAATCC CAAACAGAAA GCCTGAGCCC TGCCTGGCGC 840
TTTCGCGGCT GCTGGCACGG CTGCGCAGAA ACGCCAGCGT CCCTGGACCG AGCGCGGGGA 900
GGGGCAGGCT TCCAGCAGCG CTGTCCACTG GGAAGAAGAC ACAACCCACA TTTTTAGATT 960
TTCCAGTTTC CACGTTGAAA AAGCAAAAAG ACATGAGATT GATTTGTGAC CCAGTGTATC 1020
AAAAATATTA TTTAACCGAT TAATCAATAT GAACAATTGT TCATTAGATA TTTTACTTGT 1080
TTTTAGGACT ACGTTTTCAA AATCCGGTGA GAATTTTATA CTCACAGCAC ATCTCAGCGC 1140
TGCAGCTCAC GCAGGGGCGC CTCCAGCGTC AGGCTTTCTG GGCTCCTGGC TGCGTGCTGC 1200
TGGGCACGTT GCTTAATATG GCAAAGTCCC CATTTTTCTC ATCCAGAAAA CGGAGATCAA 1260
AGTACAGGTG CCAATTTCAT AGGACTACAG TGAAGATCAA ATGAGAGAGC TCAGCCAAGA 1320
ATATAAGACC CATGCATGGT CTGTGGAAGT 1350
|
