| Tag | Content |
|---|
EnhancerAtlas ID | HS105-45319 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:128158220-128159390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr2:128159346-128159357 | CTCTGTGGTTT | + | 6.14 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23461 | chr2:128157816-128160429 | Colon_Crypt_1 | | SE_24012 | chr2:128158103-128160336 | Colon_Crypt_2 | | SE_24894 | chr2:128157929-128160865 | Colon_Crypt_3 | | SE_28345 | chr2:128157679-128161035 | Fetal_Intestine | | SE_29146 | chr2:128155181-128161071 | Fetal_Intestine_Large | | SE_43376 | chr2:128158101-128159246 | Lung | | SE_50833 | chr2:128157885-128160708 | Sigmoid_Colon | | SE_52838 | chr2:128157292-128160895 | Small_Intestine |
|
| | 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 |
| GH02I127400 | chr2 | 128157999 | 128160842 |
|
Enhancer Sequence | TCCTAAAATA GTACCTGTGA CCACGCCCCA CGGTCTTAGA CCTGGGCAGG GCAACTGTGC 60
AGACAGCAGG CCCAGCCAGG AAGCAAGCTG GCAAGGCGTT CTGCAGCGAA GGTGAGTACC 120
AGTGATGCAA GGTGGAATAA GAAAAGTGCC CTTTGGAGGA GTCACTTATG AGGGGAATGG 180
GGAGCAGGGC AGCAGAGGCC CCTCTGCTGC TGGGAACCGG GCGCACTCCC GCCAGTCGCA 240
GGAGCTGGCT CCACCCGCCC CTTCTGATCC AGTGTCCCGC AGTCCTGCCC GCTTCACCGC 300
CCTCGCCTAG CCCCCGCGGG TGGTAAAAGT CCAGCCCGGC GGAGCGCCCC TGCCTCCTTC 360
CACGCCCCTG GCCTGCCCTG CGCAGCTACG CCCAGCCCGC GTCCATCCCG GACCATCCTG 420
TTGAAGGCAG TCCCCTGGCA CGCAGGGCTG GGAGCTCTTA GCTGAGGATG GAACCGACTG 480
CACCAGGAGC CGCTGGGAGG AAGGCCGAGG GGCGCAGAGG AGAGGCAAGG AAAAAACAGC 540
AGCCCAAGAA TCGGGCCTCC CTGTTACAGC AGGAGTCGCA TCTATTTATA TATGTTATGT 600
CTTATTGCTC AGCAACCAGC TCTCGGCCGG GGCGTGGGCC GGGAAGAGGG GTCTCCTGGT 660
GCAGCGGGTT GGCGTGACTC ATCACCGCCG CGCACTCTGG CCTCTGGGCC TAGGTTAACA 720
GACTCCCGGG TTTCAGGCTG GGCCCAGGCG GCCAGGCCCT CCCTGCTGAG GAATCTGGGT 780
TGGGGCAGTG CCAGCTCCCT GCTTCTCACC TGGCCACAGA AGGGGTAGCG GGAGGAGCGT 840
GGGTTCATGG AGGCAGGTGG ACCACCCCTT GGCTCCTGGC TCTGCCACCT GTCCACTGTG 900
TAGCCCTGGG CGAGTCACAG CCTCTGACAT CAGCCTGCTT ATACTGTAAA AGGAGTGTGA 960
GATCATGTTG GAGGAGACAC TACAGTGAAA TCTAAATACA TTTTAACTCT TCACACACCC 1020
TCTCCCATGC ATTTGACAGC GAGGAAACTG CAGCCCGGGG CAAAGTTGAC TCACTTCCCA 1080
AAGCCAACTA ATTTGTACTT AGAAGAGGCA GGATTTGAAC CGGGGCCTCT GTGGTTTAGA 1140
GCCCTGTGTA TCTTATCACT GTAACGCCTA 1170
|
