| Tag | Content |
|---|
EnhancerAtlas ID | HS180-41818 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr6:36797520-36798790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr6:36797940-36797955 | TGAACTCTGAACTCT | - | 6.11 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_30666 | chr6:36797571-36798903 | Fetal_Muscle | | SE_41488 | chr6:36797604-36798853 | Left_Ventricle | | SE_48751 | chr6:36797595-36798779 | Right_Atrium |
|
| | 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 |
| GH06I036829 | chr6 | 36797514 | 36798647 |
|
Enhancer Sequence | AGAGGTTGCA GTGAGCCGAG ATCACGTCAC TGCATTCCAG CCTGGGTGAC AGAGTGTGGC 60
TCCATCTCAA AAAAAAAAAA AAAAAAAAGT TGAGTGTAGG AATTGCAAAA AAAAAAAAAA 120
AAAAATACCC AACAGGAATC CTGATGGTCC CACAGAGGCC CCTGAGGTAC TGACCAGCGT 180
CACCCCATTT CTGCATGGAG CAATTTGCAT AAACATCTGG CAAATGGAGT GGGAGAGAGA 240
TGACACCCAA CAAGTATATA ATCTGTGCCA AGTCCTTTGT CATGTACTTA GCCTGTGACA 300
CTCTATTTAC CCTCCATATC AACGCCAGAA AGTAGACTTT GCTCCCATTC TATAGGCAAG 360
GCCACAGAGG CTGAGCGATG TGCCTGATGT CACCGGCTTG TCAAGAGGCA TGCAGAAATG 420
TGAACTCTGA ACTCTGAAGC TCAAGCTCAT TTAAAGGTGC CCTGGGGAGT GCTTGCACTA 480
CCAAAGCCAA GGACTCCCAA AGCCCCATCT GGGCCAGCAA TGCTCCGTCT TATCCTCACT 540
GTCCTGCTTC CCATCCTCAG CCTCTCGGAG CTGCTCCCAA ACAAACGACT GAAGAGGAGA 600
ATGGGAGGGT TTCCCATGTC CTCCTGCCCA GCTCCCAGAC CTAAAAGGCA GAAGTAATCC 660
GAGGAAAGCA GGGCGGGAGC TGGGAGGAGA GAAGCCTTGG CACCTAGCCC CTGGCACTTA 720
CCCATCTCCC CTTTCAGATC CTGTTCTCAC CCGCGTGCTC TGCTTCCCTG CCAAGCAACC 780
TCACCAAGGT CTAAAAAGCA ATTTTCACAT GGCTTAAAGA GCTCTCCTTC CTGGGGCAAT 840
TTGCATTTTT ATTGTTATTA ATTATTGTAA TAATTGTCCC TCTCACACTA CATGGCCAAG 900
GGAAAAGAGC AGGAGCTCTG GCCTCAGATG CTTCTGAGCT GGAGTCCCCA CATGGCGACA 960
TGTGGCCCTG ACAAGGTGCT TCATCTCAGT TTCCTCATCT GGGCATGGGG TCACATACCT 1020
GCCTGTGGAG TTGCTGTGAA GTCAACAGCT TCAAACAGAA ACGTAGGAAG CACACTCAAT 1080
TCCTCTCTTT CCCTTATTCC CCCTCCTGTC CCATCAGCAA GTTTTAAATG TTTCTACTTC 1140
AAAATATATC CCAGATCTGT CCACTCCTCC CCATGCCACC ATCAGTATCA TCTCTCACTT 1200
GGAGGCCTCA GTAGTCTTCT GCCTAGCAAT GTGCTTCCAT GCCTGCCTCT CTCTACCCTT 1260
CATCAGTCCC 1270
|
