| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00337 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:15347310-15348780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr1:15347458-15347469 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr1:15347458-15347469 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr1:15347458-15347472 | TTTCTGGGAAAAGG | + | 6.15 | | TFAP2A | MA0003.3 | chr1:15348639-15348650 | TGCCTGAGGCA | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_06289 | chr1:15346844-15348291 | Brain_Hippocampus_Middle | | SE_06289 | chr1:15348360-15353330 | Brain_Hippocampus_Middle | | SE_26798 | chr1:15346792-15353359 | Esophagus | | SE_53292 | chr1:15346056-15353406 | Spleen |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I015019 | chr1 | 15346085 | 15348811 |
|
Enhancer Sequence | GCAAAAACGC TGGCATGATG TGACTTGCCC CAGGTCCCCC CACATCACTC TAAGGAGCGG 60
CAGAGCTGGA TGTGAACCCA GATTGTCTGG CTCCGGGTTC TCACTCGTGA GCTCTGCTCT 120
CTGCAGCCTC TCTCCTCTCT TGTAAACTTT TCTGGGAAAA GGCTGCTGCC TGCATCTGCC 180
TTCAACAACC CTGCTGTGTC TCTGTTACGC AGCAGGGGTG AGACCAGTCC ATATCACTAG 240
GCACCCAGGG CAGCTTCCCG ATGGACAGTC TTGAGTAGGA CACCAAAACC CAGAGAGGGT 300
GCCTGAGTTC CCAAGGCCAC ACAGCATGCG GGTTTGCACC CCAGTGTCCT GCCTCCCTGT 360
CCACCGGCCA TTCCCTGCTC CATGCTGCCT CTTCCTCCTT TCTCAAGACC GAGCCCAGGC 420
CATTATCTTG CCTGCATACG ACCTCACACA CCCACACAAG CCTTTAAAAA TAGTCCTCGT 480
TGTGTGGGGC ATGGGGCCTG AGGCTGATAT TGCATTTCCA GAAATCTCCA TTTCCCCCTC 540
CCGCTTCAAC CTAGGGAATG TCCGTGTTCC GGGCCCATTC CCTGCCACTA TTTTTAGTGG 600
TGATTGGGAG GAAGGAGGAC ATTTCCTGGA CTCCCCTTCA GAGGCTGGAA AACAAACACC 660
ACCCGCTCCC AGTCCCGGCC CCTCCCATTT CCCTCCTGCT GGTATACCTT GGCCTCCTGT 720
CTCCCTCGGG GAGGAGCAGG CAGTGGGGGC CTGCTTCCCG GGGCCCTCCG CCCTCCTGGC 780
TTCCAGGTGA CCTCTGAGCT CTTCCAGGGG CAGTCCTGAG CCGGGGTGGT GGCAGGGACA 840
GTGTGCCCTG CGTGCAGTTA GCACCCTGAA GCCTGCAGAG GGCCCCTGTG GCTCCCTGCA 900
GTCCCTCTTA TGACGGACAC TCTGTCTGCA GGTTTCGGTC CCCTCCCTGG GACCGGCCTA 960
GCTGTTTCCA GCCCTTTCTC ATTGGAAGCC CTGGCTCCTG GCATCTGTAT GAGTTCGTTT 1020
TCATGCTGCT GATAAAGACA TACCCGAGAC TAGGACATTT ACAAAGAAAA AGAGGTTGGG 1080
GAGGCCTCAT AATCATGGCG GAAGGCAAAA GACACTTCTT ACATGGTGGC AGCAAGATAG 1140
AGCATGAGAG CCAGGGGAAA ACCATCAGAT CTCGTGAGAC TTATTCACTG CCATGAGAAC 1200
AGTACAGGGA AAACTGCCCC CAGGATTCAA TTACCTTCTA CCATGTCTCT CCCATAACAC 1260
GTGGGAATTA GGGGAGCTAC AATTCAAGAT GAGATTTGGG TGGGGACACA GCCAAGCCTC 1320
ATGCATCCAT GCCTGAGGCA GAGGCTCTCC AGATGGCCAG GACGGGCCAT GCACCCCCCT 1380
CCCTCCCATC ACTTCCCTGC CCTGGCTCCA AACGGGTCTA TCCAGTGGTC TTGCAGCTCT 1440
GCTGAGAACC ACGCCCGCAC CCCGCCCCAG 1470
|
