| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00373 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:8214180-8215280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr1:8214829-8214845 | TCTAGAGTAAACAAAC | + | 6.24 | | IRF1 | MA0050.2 | chr1:8214403-8214424 | TTTTTCTTTTTCTTTCCTTTT | + | 6.52 | | MEF2A | MA0052.3 | chr1:8215178-8215190 | TCTAAAAATAAA | + | 6.07 | | MEF2C | MA0497.1 | chr1:8215176-8215191 | TATCTAAAAATAAAA | + | 6.26 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_34231 | chr1:8213424-8217568 | HCT-116 | | SE_47106 | chr1:8213490-8217641 | Panc1 | | SE_54673 | chr1:8213879-8215466 | Stomach_Smooth_Muscle | | SE_65889 | chr1:8214070-8216395 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 8214738 | 8215135 | | chr1 | 8214748 | 8215059 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I008151 | chr1 | 8211363 | 8216436 |
|
Enhancer Sequence | CGGATAGAGG CCCATGGCGA CAGTTGTGCC AGCAGATTCC TGCTGCTAAG TCCCCGGCCT 60
TTGCGCTCTG TGGCCTGGGC TGATGGGTGG GTGGGTGCCT TTATTTGCCT GGTTGAGGAG 120
TGCACTCACT GGGGGCCATT TGGTTTGAAA CATTTTTTGC AGCTAAGGGG TGGTAAAGAT 180
GACGCTAGTT TAGCTGAGTT TAAGGCTAAT TAATCAGCCT TCTTTTTTCT TTTTCTTTCC 240
TTTTTTTTTT AGACAGAGTC TCACACAATT CCCTGGGCTG GAGTGCAGTG GTGCGATCAT 300
GGCTCACTAC TGCAGCATCA ACCTCCTGGA CTCAAGCAAT TCTCCTGCCT CAGCCTCCCG 360
AGTAGCTGGG ACTATAGGTG CCCAACACCA TTGCCCCGCT ATTTTTTTAT TTTTTATTTT 420
TTATTTTTTG TGGAGACAGG GCTTTGCCAT GTTGCTCAGG CTGGTCTCAA ACTCCTGGGC 480
CCAAGTGATC CTCCTGCCTC AGTCTCCCAA AGTGCCAGAT TTACAGGTGT AAGCCACCGC 540
GCCCAGCCAA ATCAGCCTTC TAAAGAGCTT AATTTTCCAT CACTGACTTT GTGTTCTTTT 600
ATACAAAGGT TGCAGACTCC GAGGCTGAAA CCCCTTTCTG ACCGGTAGCT CTAGAGTAAA 660
CAAACGCCTG GACTTTCTTC ATCCCCTGAA GACAAAGAAC TTGTTCATGA GCCTCTCCAG 720
GCAGCTCGTG GTCTGAGCTG TCAGGAATGA CGGATGAGCA GCTGCTTTTG CCGGCGCCTC 780
CGCGGCAGCT AAGGTAGCGC TCACAGGACT GTCTACACCA TGGACTCAGT GTTCAGGTGT 840
TCAGGGAGTT ATTATTGGAG CAGCTCACTC TATCTTAAGG CAGACAGCCC CGGGCAAAGC 900
GCAGCGGATA AACACAAGTG ACATCTTATG AAACCTAAGT TCATGTGAAA TCCTAGATAA 960
TTCTGTTGTC AGAAGTGAAA ATATATATTG CATTTTTATC TAAAAATAAA AATGAATGTG 1020
ATGATCTTTT TGCTCTTTGA GATCTAGATT TCGAAAATCT TTTCTTAGAT GAAGAAGGAA 1080
GCCATTTCTT TGTACTATAT 1100
|
