| Tag | Content |
|---|
EnhancerAtlas ID | HS191-00182 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:9339340-9340420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:9339393-9339408 | GGAGAGCAAAGTTCA | + | 6.3 | | RARA(var.2) | MA0730.1 | chr1:9339757-9339774 | AGGTCATGCAGAGGCCA | + | 7.09 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_00563 | chr1:9337903-9340328 | Adipose_Nuclei | | SE_23490 | chr1:9337921-9342330 | Colon_Crypt_1 | | SE_23818 | chr1:9337980-9341807 | Colon_Crypt_2 | | SE_24876 | chr1:9337785-9342445 | Colon_Crypt_3 | | SE_50208 | chr1:9338047-9342398 | Sigmoid_Colon | | SE_52461 | chr1:9338392-9340456 | Small_Intestine | | SE_65576 | chr1:9339233-9340062 | Pancreatic_islets | | SE_65576 | chr1:9340212-9341781 | Pancreatic_islets |
|
| | 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 |
| GH01I009278 | chr1 | 9338461 | 9342291 |
|
Enhancer Sequence | TGTGTTTATA ACCAGAGCCT TACAGGCAGT TGGCTCCAAC GCCCACCTGC ATTGGAGAGC 60
AAAGTTCACA GGAGACTGAG GTGGGAGGGG AAGAAGCCTC TTCCTGCTCT GAGAATCCGC 120
ATGGGTCGCA GTGCTTCCCT TCCTCAGCTC CCCCACCGCA GGCTGCTAAA ATGACCCCGA 180
GTGCCTCAGA AATCTCAGGG CCACCGCAGC CTCTCCCCTC TCAGCCATGG TTCGATTCCT 240
CATAAATATT AAGACTTCAT GTGCTCCTGC GTGGATTTTC ACCAAGTCCT AAAATGCAGT 300
GTAGACGCTC CAGGGAAGAG GAAGCAAGTG ACATTCCTGG CCCGCTCTTA CGCCACGAGC 360
TCTGCAGACG CCGAAAGGTT GCTCACAGGA GGCGGAAAGT GCCAGGGGTT GGGCCTGAGG 420
TCATGCAGAG GCCAACTGTG GGCCGGGGTC CCAGCGGCAG CCTCCCCACC GAGGGCTGTG 480
TTGAACCCTG GAGAGAGAGG GCGAGAGAGA GAGAGCGAGA GAGAGAGAGA GAGAGACAAA 540
GCGAGCGAGA GAGAAAGCTA GCATGAAGGC TTGTTGGAGG CCTGACTCCC CAAGGCCAGA 600
CCCTAAGGCC TTGAAGGTCA GCCAAGAAGT TGACCAAGCC AAGAAGTCCT GAGACTTGGA 660
GCCACAGGGC CAGTGGGGCA CCATCTCCCC AGAACAAAAA CTGTACCCCA AGAATTGAAG 720
GGAAATATTA TTTTTACTCT GAAACGTTCT GGAGCAGAAT GCAAAATTCC ATCCCTTTCA 780
AATAGAAAAC ACAAGCTATT CACACTTGAG GTGGGTGAGG GTGCTTTTGG GGAAAAGTTT 840
GAGAGTCGCG TCCTGGGCAC TGGGCAATCA TCAGAGGGTG TCTCCCTCGG GAGGGGTCCA 900
GTCAGGCCTG GCTTCACGGG GATGGTCAGT GAGGCAGGGC TGGGCGATGG GCGCCGGCTC 960
CTCCTGGAGT CAACCTTTCA TTCATTCATT CATTCAGCAA ATGGCAGTCG TGGGGTAGGC 1020
AGCCATGCAC ATGGCAGTCA AGGCCCTCCC TTTCCATTCC AGACTGTGAT TGATCCGTGC 1080
|
