| Tag | Content |
|---|
EnhancerAtlas ID | HS048-27480 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr4:26085180-26086510 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr4:26086406-26086419 | ATGACCTCATTTT | - | 6.2 | | JUND(var.2) | MA0492.1 | chr4:26086405-26086420 | GATGACCTCATTTTG | - | 6.17 | | POU2F2 | MA0507.1 | chr4:26085466-26085479 | TTTATTTGCATAT | + | 6.98 | | Pou2f3 | MA0627.1 | chr4:26085465-26085481 | TTTTATTTGCATATAT | - | 6.13 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_59332 | chr4:26050417-26092107 | Ly3 | | SE_61195 | chr4:26051599-26096077 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I026083 | chr4 | 26085160 | 26086610 |
|
Enhancer Sequence | AGGAATTGGG TGGGATGAGA TTTGACCCAA GGACTTGGGG TATGGTTGGT CATGGCTGAC 60
ACTGAGCTTC ATTTTTCCCT CTCTGCACTG AAATTTTTTC AAGCTTTCAG TTGAGCCAGA 120
AAGCCTCATG TTAGCATTGT CTTGGGGTGA AGGGAGGCAC TGAATCCATT GGATCAGGGA 180
CACACATCCA GGTGGAGAAA TGGTAAGTGA ATGCCAAGAC TGTGTCTACA TTCCTTGGAA 240
GAACCCTGGG CTTCCTGAAG CCTCCTGGTT TGGAAGCTGG AGTTCTTTTA TTTGCATATA 300
TATATATTTT TTACAAAAAG GATGGTCTTG GAAGGTTGTC ATAAACTCAG GGACACAGGA 360
GTTCCGTCTC ATTGTTATAT TTCAGGGACT GAGACTTAAG ATGTTCTGCA GGACAGCTGA 420
AACCATGGAG AAGGGTGCTT TTTAACAGGG TTCACCTGTT CTGAGGACTC TGCGACCACA 480
AGCACTTGGC CGCTGTCAGC AGGCTAGGTG ATTACAGCAT TAGATCATGC CTCTAATGGG 540
AAAAAGGCTT CTCCTTTCTG GCTGACTAAT CAGCTTGCCA TTTTTATTGC ATGATCAGTA 600
TCAAGAGCCA ATGATTTCTG TCAGCTCCCC GGGTGCACAC TAGCATGACA GAAAGAACAG 660
CTATATTAGC AAAGAAAACA GGTGGAGAGA TTAGCAAACT CACTTAAAAG GTCAAGACAG 720
CTTGGTCCCT TATGGCACAG TGACAGGAAG GCTGAAGGGG CCCCTTTCTT AGAACAAGAA 780
TAGCTGCTAG TACGAAACTC CCATACTTCT AGTCATCTAT CTAGTCATCT TGCTATTTTC 840
CTTTTTCTTA TTATTTTAAA GTCCAAAGTA TTTCATGCTC ATTGTCAATC TGTAGCAGTT 900
CCCTAGGGCT GCCATGACAA ATTACTACAA ACTTGGTTTC TTAAAACAGC AGGAAATTAT 960
TCTCTCATGG CCCTGGAGGC CAAAAAGTCT GGAATCAAGG TGTGGGCTAT GCTCCCTCTG 1020
GAGGCTTTAT TGAAGAATCC CTCCTTACCT CTTCCAGCCT CTGGTGGCTC CAGGCAATCT 1080
TTGGCATTCC TTGGCTTGTG TCTGCGTCAC TCCAATCTTT GCCTCCATCT TCGCACGGCC 1140
CCCTCTTCTC CCTAAGTGTC CCTTCTCTGC GTTTCTCACA TAAGGACACT TGCTGTTGGA 1200
CCTAGGGCCC ACCTGGATCA GCCATGATGA CCTCATTTTG AGATCCTTAA CATAATTACA 1260
TCTGCAAAGA CTCACTTTCA AATAAGGTCA CACCCACGGG TTCGAGGAAG ACATGAATTT 1320
CGAGAGGTCA 1330
|
