| Tag | Content |
|---|
EnhancerAtlas ID | HS050-71670 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chrX:41271170-41272210 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:41271905-41271923 | GGAAAGAGACAAGGAAGG | + | 6.03 | | HNF4G | MA0484.1 | chrX:41271696-41271711 | GAAGAACAAAGTTCA | + | 6 | | HSF1 | MA0486.2 | chrX:41271548-41271561 | GAAGGTTCTAGAA | - | 7.12 |
|
| | 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 |
| GH0XI041411 | chrX | 41271181 | 41272493 |
|
Enhancer Sequence | CGGTGGATCA CTTGAGTCCA GGAATTCGAG ACCAGCCTGG CCAACATGGT GAAACCCCAT 60
CTCTATTAAA AATACAAAAA TTAGCCGGGT GTCATGGCAC GCACCTGTAA TCCCAGCTAC 120
TTGGGAGGCT GAGGCACAAG AATCGCTTGA ACCTGGGAAG TAGAGGTTAC AGTGAGCCGA 180
GATCGCACCA CTGCAGTTCA GCCTGGGCGG CAGATCAAGA CACCGTCTCA AAACAAAACA 240
AAACAAAACA ACTTCAAGAA TAATCAAAAT CAGCTTCATT CACAGGCTCA CAGGGTAGAA 300
GACCAAGAGT CACCTTCCCT AAGTGAGAAG TCCTCTGCAG ATTTTGCATT GGTAGGCAAT 360
CTCAGCTTCT TGCACAGAGA AGGTTCTAGA ATCTCCCTAA GCATGGGGGT GGGGGCAGGA 420
GATGTGATGG GGCACACCCT TATGAAGCGG AGAACTTGCC AGCTGCTGAA ATAGAATAGA 480
GTTCAGAGCT GAAAAGGGCA GGGAGGGTGG AGACACCTGG CTACCAGAAG AACAAAGTTC 540
AGTCCAAGCC CAATTGTCCT TTCCTGGCCA GCTGCCAACC TGCTAGCCTA GGCATTCTAA 600
ACTTTAACAT TTAGTAAAAT GGTCTCAAAT TGGAGAGAGA GTGTCTCTTC TCCTGGAGGA 660
GTGGAAAATG ATGTTGTTCA GTCAGGCCGA GGTTAGCAAC GTTAGCAAAG CCCTCTCTGT 720
CCCTACCTGG TGGCAGGAAA GAGACAAGGA AGGTCTCAAA GATGGATGCC TTGCTACCTT 780
CCTGCAGGCT TTGGGTCAGG TTTGGCTAAG CTATCATTAG CTGTTTCCTG GTTGATATTC 840
AGCTGTAGCC GTGGTGGCAC TTCCTACACA AGCACTGATT TTTCCTCATG TTTGTAAAAC 900
CGGGGCAAAA CTTGGTAAAC TTACTCTTGC CAAAGTTCTG GATGCTTACT TCCCTTTTGA 960
ATTCTTTTTT TTTTTTTTTT TTGAATCTCA CTCTGTAGCC CAGGCTGGAG TGCAATGGCG 1020
CAATCTCAGC TTACTGCAAC 1040
|
