| Tag | Content |
|---|
EnhancerAtlas ID | HS060-24117 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:42133050-42134480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr3:42134407-42134418 | AAGCCATAAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_00063 | chr3:42131608-42135031 | Adipose_Nuclei | | SE_10922 | chr3:42129314-42141993 | CD20 | | SE_26989 | chr3:42132020-42134253 | Esophagus | | SE_40683 | chr3:42131838-42134266 | Left_Ventricle | | SE_65044 | chr3:42132075-42135151 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGTAAGTTT GTTTGCCAGG TCTGTCTGCT GTCTGTTTTC TTTGTGGTGT GGTCGGAAAG 60
GAGAAAAGAC CACAGGAGAA GCTGTCTCTC TCTTGCTCCG TGCTGCTTGG GAGGTTGTTC 120
ATGGTCATGT GGTAGAGAAA TTGCCATGTT GAATGATAGG CAGAGCAAAG GGACTTCAGA 180
GACACAACTA CTGCCCTCAC CACCCCCCCA TCTCCCGTTC CCAGGTCCCC TTGTCCCCTT 240
GCCCAGGCTC AGTAGGTGCA AGTGACACTT GCAGGGCATG AGCACAGGGC TGAGTTGAGC 300
CCAGACCCCC TGCACTGCCA CTCCCTTTCC CTTCACAGTT CTCTGCAGTG GGTGGACAGG 360
GTTTCTAAGG CCTCCTCCGC CTCTCCAGCT CTGATTTCTC TAATCCTATG TCTTGTCTTT 420
ATCCTGATTT CTTAGATGCT AACCTGGTAT CTTGGGTCAG CAAGGAGTTT TTCAGAAGGT 480
GAAGGACAGA GTTAGACTGT CTCCCTCCCT CTCTCCCGTT TCCCTCTCTT CCACCCTCCC 540
TTTCTTTTTT GTCCTTTACT AAATGCTTGG GCCTGGGACT CGGATCCACA CCCCAGTGAT 600
GGAGGGCTTG CTAATCAGAT CTGCTGTGGC TTGTGTCTCT TGCTGTGGGG CTGACACCTC 660
TCACTTCCTC TAAGCTGGTC AGAGTCCAGT GGTTGATGAC CCATCTGGTT TCTGTCCTGT 720
CTACACGCTG CTTCCTGAGA GCTGTCTGGG CCAGAAAACA GTTAATTCCT GAGAGAAGTG 780
AGCTCCTGTT CCATTCCAGT CAGTTTTAGG CTTTAAAACA TGTAAATCTT ATTGAATAAG 840
CCTAAAGACA CTTCAAACAT GCATCTTACT GAGGCAATCG TACTTATTTT TGTGTGTTGA 900
AGCAGCGTGC ACCCAGGGCC AGGTTTTTAC TGGGGTTTAT GTTAATTCCT GGGGTCAGAG 960
AGAGGACTGG TCCTGCCCTC AGAGCACAGA GGTGGGCCAG GGTGTAAAGG AGAAGCTGTA 1020
AACCGAGTGA GAATTGCCTA GGAAAAATCT GCTAACAGGA GTAGCCCTGC CTGGGAGGAC 1080
TCTTCATCAA AGGGCCATGG CTTAGAATTT GTTCCTTTTA TTTTGTTGTG TTGTGTTGTG 1140
TTGTGTTGTG TTGTGTTATG TTATGTTATG TTATGTTATG TTATGTTATG TTATGTTATG 1200
TTATGTTATG TTATTTCGTG ACTCACTGTA TTGCCCAGGC TGGTTTTGAA TTCCTGGGCT 1260
CAAGTGATCC CCCTGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCATG 1320
CCTGACCCAG GATCTTTTCC TTTTCTATCA CTGATTTAAG CCATAAAACT TGATGTCTTA 1380
TCCTCTGAAA ACATGCTCAA ATAAAACATT ATGGAATTCT TACACATCTT 1430
|
