| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01676 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:214149940-214151270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr1:214150442-214150457 | GGTTAATTATTGACT | + | 6.07 | | HNF1A | MA0046.2 | chr1:214150442-214150457 | GGTTAATTATTGACT | - | 6.68 | | HNF1B | MA0153.2 | chr1:214150443-214150456 | GTTAATTATTGAC | - | 6.25 | | HNF1B | MA0153.2 | chr1:214150443-214150456 | GTTAATTATTGAC | + | 6.41 | | ZNF263 | MA0528.1 | chr1:214151057-214151078 | GGGGGAGGGGGAAAGTGGGAG | + | 6.52 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_65842 | chr1:214150319-214151482 | Pancreatic_islets | | SE_68033 | chr1:214146367-214176127 | TC32 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I213976 | chr1 | 214150320 | 214150779 | | GH01I213977 | chr1 | 214150941 | 214151090 |
|
Enhancer Sequence | ATTTCAAAAG CACTTCTCCT TTTATCACGA ATCGAAGAAG AACTAACATT GAGAAACAAG 60
GAACCAGAAT ATTTAGAGAT GCTGGGAATA AACTACAAAC TAACATGGTC AAGGGAGAGA 120
AAATATGATC CTCTCAGAAG AATAATGTAA CAACAATCAG AGCACATCTG GGATTTGATT 180
CAAACCAACC TGGAACCAGA TTGGATCTCC AAGCTGTTCT GTGTATACAC ACACACACAC 240
ACACACACAC ACACAGACAC ACACGCTGAG ATTTCCAAAA GTGAAATTTC CAGAAGTTAT 300
CCTACAGAGT TAACCCCAGA AAGGACTTCA CTGGCAGACA CAGGCATAAC TTTACTCCTT 360
TTGTGATGAC CCATGAGTGG GGTCTATGGC AGTCTGAATA GATGGGCCTT TCTGTTGAAA 420
GATTCTGCCT AATCCTTCCC ACCAAAGCAG GGTTCTAAAG GTGTCAGCAG GATTTGGCTG 480
ACTGGATCGT TAATGGAGCT ATGGTTAATT ATTGACTGAT TAGGGATTTA CCTTATCTTT 540
CCGTCAGGAG CTGGCTCAAG ACTTAACGGT AAGCAATTTA GAGCCAGGGT GAACCTACAC 600
ACATGCCTTT TTCTTCTTTT CCTTTGGGTC ACTTTAGCTT GCCCCTCCCC ATAATTCACA 660
TTCAGGACAG AATGGCCAGT CCTTACAAGG CGTGGGAGTC CTCAAGAGCA CCGAAAATGA 720
GAGGGGCCAG GTCCACGTGA CAAGTGTCCA GAGACAGAGG CTTAGAGAAA TGTGCCTTTT 780
GCAAAACAGT GTTTATGTGT AAAGGTTTTC CAGTTAAGTC CCTGGGAGAA AAAAAAAAAA 840
AAGCACTTGC TTTTTGTCTC TAAAAGGTCT GGTGATGCCC GTGGGTGAGA ATCCACCCCG 900
CACTCCCCAA GGCCCCTTGG CAAAGCCAGG GAATGAGTAC AGGCAGCTCA GGCCCAGCTG 960
CCCCAGATAA GAGGTGGCCC GTGTTAATGC ACAGGCTTCC TCTGCACCTC AGCAGGGCCT 1020
TCCTTTTCTA AACAGTCTCC CTTTAATGTT GGCGAATGTT GTTTTTCCAT TGACTCAACA 1080
TCTCGCCTGG TGGTAAGCCA GTGAGGAAAG TTGCAGCGGG GGAGGGGGAA AGTGGGAGAG 1140
AGTGATGCCA AAGCAAAAGA GCGGGACGGT CAGCCAGGTT TCCAAACAAG CTAGACACCT 1200
GCTTTGGAAA GACAGTGACC AAGCCTAGAC TTCTGGCTTC CTCTTCACTT TGATCAGCCT 1260
TTTGTTCCCT GCGGGTCTGT GATGGGCTCC CTGCCCCTCC CCTCACCACT GCCCCCTTCA 1320
CTGGGAGCTA 1330
|
