| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04504 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:162182420-162183900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr1:162182716-162182732 | TGTTCCTCGAAAGCCT | - | 7 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_47180 | chr1:162179528-162191610 | Panc1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I162212 | chr1 | 162182398 | 162184258 |
|
Enhancer Sequence | TTGTAAAAGC TTCGGGATTT TAGTGAAGCC ACACACTTTC CTGCCCCATG ATCAGTCTAG 60
GGGGTCTAGC TGTGGATGCA GGCCTAGAAA GTATCAGTGA GTGCGTGGAG GATAGCCATG 120
AGATGGCTGT GGAGAGTCTC CTACCTCTCC TTCTTCCTGC TGGGATGTTG CTTCTGCCCT 180
CGACACACCC TGTGAACTTT GGCTGCTGCC GTGTAGCTTC TGAACTCTCT GTGGAGTGAG 240
TGCCCCCGGC ACACGGCGGA CCATGTCAAC AAGTTCAGCT GTATGAGCCT AGAGACTGTT 300
CCTCGAAAGC CTGTCACACA GCTGCCTTGA GCCCAAGTGA CAAGCTGTGG ATCTTGCCCA 360
GGGTAACCAT TTCTGACTCT CCTGAATAAT ATGGGGTGGA TCTGGGGCAT TGTGTCTAGG 420
AAAAGCAGGT GGAGGGTGTC TCTAGGGGAT CAGGTCAGGG CTGGCCGCCC ACCTCCCCAC 480
CCTCAAGGAA TCTAGATACA GTTAGGGAGT CCCAGGTAAC TTGAACACCC TGGTACATTT 540
CCTTAGGAAG GAAATGAACG TATGAGCATG ACCCCTTTTG CTTTATTCCA ATACATATTT 600
AAATACCCCA GCAACTCTCA TCCACAACAT TAGCTGTGAT AACCAACTGT ATTTCCTGTC 660
TGAGACCCTT TCCTTCTCCA GTAATTAGCC TTTGTCTAGC CTTTAATCCA GTGGTGGTTA 720
TATGGGGAGC TGCCTGGTCA GGAATTTTTG CATTGAGGGA GGAGACTCTC CCACTGATCC 780
TGTGCAGGCA TTTTTGCTGA CAGATTGTTA TGGCTGGAGT TGCCAAATAC AAGAAGCAGA 840
GACCTTTCAC CTTCACCTGA GCTGTGTGCT TTAGAGAAAG AAGGATGTGC CCACCTCCTA 900
TTTTCTGTCC TCACTGTTGA ATTCGGTTGA CATTCAGTTG CCCAATCTGC AGTCATATCC 960
AACTAACTGG ATTGTTTTTA AGTTCTCCTC TGGATGAATT ATGAGCTTTC TTGACTTTGG 1020
TCAGGCTGCC TGGAGTCATT CCCAGCCTGG GCAGGTGCTG TGCCAACTTC CCTGGCATGT 1080
GCCTGTGCCT GCGGATTTTA CTATTTGACC CCTAGCTCTC CCTTGGAAAT ACCAAGCCTG 1140
GAACTCTGGA GAAGGCGCCG CCGCTCGTGT AGTTCTGAAA GGCTCTCTTT GTCCTGAGGA 1200
ATGCCTGTTG CAATGAAGCT TGGTAAATAG CCAGCTCATT TCTCCTATAA ATTAAAATGA 1260
AGGAACCTCA TCCGCTAGAA GTAACTTTAC TTGTCTCGTC TCATCTTCTT TATTCAAGCC 1320
TATTTAATGA ATATTTATTT AAGACCTAAA ATCCAGCACT GTGCCAGGCA CTATAATGGG 1380
GGACATAGAA GTAGAAGTTT GTGGTCCCTG CCTTCAAGGG CTTAAGGCTT CTCAGTGGGG 1440
ACAGGCCATG TGCACATGAA ACTATCAAAG AATATATAAA 1480
|
