| Tag | Content |
|---|
EnhancerAtlas ID | HS050-28984 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:46093220-46094030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr17:46093687-46093698 | TCTGACTCATT | + | 6.32 | | GATA2 | MA0036.3 | chr17:46093676-46093687 | TTCTTATCTTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_33576 | chr17:46088189-46094365 | H2171 | | SE_63289 | chr17:46066472-46094348 | NCI-H82 | | SE_63365 | chr17:46063975-46102323 | NCI-H69 | | SE_67063 | chr17:46088189-46094365 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATGGAGTCAC AAAGTGCTGG GATTATAGGC GTGAGCCACC ACGCCTGGCC TTTTGTTTTA 60
TTTTTGAAAC AGTCTTACTC TGTCGCCCAG GCTGGAGAGC AGTGGCATCA TCTCATCTCA 120
CTGCAACCTC TGACTCTGGG GTTCAAGTGA TTCTCCTCCT TCAGCATCCT GTATCCACAT 180
AGAATTTAAA GGAAACTCCA AATGCACTCC CAGAACTAAA GGGAGTACAG AACTAAAGAG 240
TCACACTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTCAGT TTTCAAGATG GAGTAGTATC 300
AATCTCAGGC CCTGGAAACT GCCCCTGGAC TAGTTTCCTG GCATGCTTCT CCAGCCTTTG 360
TAAACAACTG TTTCATCTGC AGACTCCCTG CATCCTAATC CTCCTTGGGG CTGGAGGTGG 420
GAGGGTATGG GAAGTGTTCT GCAAGGTACT CCAGTCTTCT TATCTTCTCT GACTCATTTA 480
GCTACTGCCT GCAAAGTTTC CACTGGAATC TGGGGAAATG GTCTGATCCC TCATCGCCTT 540
CCTCCATATA CAGCTGCCTA CCCATTAGAC TAATCCCAGC CATTTGTCAG TCACGATGCT 600
CCATCATACT GGCCCCAGCA AACTTTCTGG TTTCACTAAG AAATAAATAG GAAGGGCAGG 660
CCCACTGGGT CCAGGATAGT GCCCTACAAG GAGACCTTTC TTCAAAATGA AATCCATACC 720
TGGGTTCAGG CCGCATTGCT TCTGCTCCCA GCACCCGAGA GCATCCTCAA TCACCTCACA 780
AGTGGGAATG ACAACGCCTG CCTCCTTCAC 810
|
