| Tag | Content |
|---|
EnhancerAtlas ID | HS098-06006 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:5670100-5671200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr10:5670470-5670491 | GAGCAGAAAGAGAAACTATTA | - | 6.04 | | MAFK | MA0496.2 | chr10:5670847-5670866 | TACTGCTGAGCCAGCAATG | + | 6.25 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_01811 | chr10:5669183-5671668 | Aorta | | SE_24448 | chr10:5670389-5670938 | Colon_Crypt_2 | | SE_26546 | chr10:5669678-5671674 | Esophagus | | SE_30703 | chr10:5669957-5671611 | Fetal_Muscle | | SE_55779 | chr10:5669761-5672216 | u87 |
|
| | 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 |
| GH10I005628 | chr10 | 5670142 | 5672550 |
|
Enhancer Sequence | TGAATTTGGA GGAGGCCTAA TTAAGTCTGT AGCAGGCATT CCCAGCAATG CATCAAAAAA 60
CAAAAACAAC AAAAAAAAAA CACGGAAGGT TGGAAAGAGA ATGCAGTGAG GAAAGGGTCG 120
GAAAGGGAGG GGCTGTGGCC AGGACGGGTG TCAGAGAGAA CTGCCAAAGA GATTCGAAAA 180
CCAGGGACCC AGATCATCCT CCGGGCCACT CCCAAATCAA GGGAAGAGGC TGGACGGGTC 240
CAGGGTCGTC TCCTTCTTTT CTGTGTCAGA TCTCCTTGAT TCTACACTAA CTCCAGGCAT 300
CTTTCTTCCT GTCCTATCCA GTCCTCACCA TAGACTCATT CTGGAAAGCG GGGAGGGATG 360
GCAGGAGAGG GAGCAGAAAG AGAAACTATT ACGCTGTAGG TCCCGGAGAA CACTGCTCTC 420
CCTGGGTCTG GGAGCTTAGG GACTTTCTGC CACACCCCAC GCCTCACAAG ACTGAAAGAG 480
TTTCATCAGG GTCTGAGCTC TGGGATTTGG AAACACTCAT GGAAAACAGA GCAGAGCCTG 540
AGTTTTGCGG AGAATCCCTG CCTTCTCCTA AAATACTCCT GGAGGAGGCA GCATCAGAAT 600
GCATGCTTGA GACGCACCAC AGGATCTGCT TCCCCAAATC CTCAAACACA CAGGACAGAT 660
GCCTCCTGGT CCCCATCATA ACCCATCAAT CACGCCCCAA AGCCGCCTGA GCCCTCACCT 720
CCCGACTCTC CGAAAGCTGC CAACAATTAC TGCTGAGCCA GCAATGCATA ATAGTCTCCT 780
TTCTGCCTTC CCGTCTCTTT CTGTCTTTTG TTCCCTGCCT GGAAATCTAT ATAGCATGAA 840
AGGAGCTGTT GAGGTGTGTG TGGTTTTTTT TTTACCAAGA ATCGGAAAAT TTGAGTCATC 900
TTTTTACAAA GTTAGACTGC GAAGGTTGTA GTCCTCTCTA AGGATTTAAT AATGAAGTGA 960
AGAGACCAGA GGTGACCAGA AACAAGTATG AGAGGAAACG AGAAGCCGTT ATTCATGGAT 1020
TTCCTGCAGT GTGCTCAGCA CAGTACTACT CTAGGAGTTG GAGGATTTTT TTTTAAAGTG 1080
GTGGTGCTAG GGGCTGAGTG 1100
|
