| Tag | Content |
|---|
EnhancerAtlas ID | HS176-28732 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:26085270-26086700 |
SNPs | | Number: 2 | 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 | AAATTTTTTC AAGCTTTCAG TTGAGCCAGA AAGCCTCATG TTAGCATTGT CTTGGGGTGA 60
AGGGAGGCAC TGAATCCATT GGATCAGGGA CACACATCCA GGTGGAGAAA TGGTAAGTGA 120
ATGCCAAGAC TGTGTCTACA TTCCTTGGAA GAACCCTGGG CTTCCTGAAG CCTCCTGGTT 180
TGGAAGCTGG AGTTCTTTTA TTTGCATATA TATATATTTT TTACAAAAAG GATGGTCTTG 240
GAAGGTTGTC ATAAACTCAG GGACACAGGA GTTCCGTCTC ATTGTTATAT TTCAGGGACT 300
GAGACTTAAG ATGTTCTGCA GGACAGCTGA AACCATGGAG AAGGGTGCTT TTTAACAGGG 360
TTCACCTGTT CTGAGGACTC TGCGACCACA AGCACTTGGC CGCTGTCAGC AGGCTAGGTG 420
ATTACAGCAT TAGATCATGC CTCTAATGGG AAAAAGGCTT CTCCTTTCTG GCTGACTAAT 480
CAGCTTGCCA TTTTTATTGC ATGATCAGTA TCAAGAGCCA ATGATTTCTG TCAGCTCCCC 540
GGGTGCACAC TAGCATGACA GAAAGAACAG CTATATTAGC AAAGAAAACA GGTGGAGAGA 600
TTAGCAAACT CACTTAAAAG GTCAAGACAG CTTGGTCCCT TATGGCACAG TGACAGGAAG 660
GCTGAAGGGG CCCCTTTCTT AGAACAAGAA TAGCTGCTAG TACGAAACTC CCATACTTCT 720
AGTCATCTAT CTAGTCATCT TGCTATTTTC CTTTTTCTTA TTATTTTAAA GTCCAAAGTA 780
TTTCATGCTC ATTGTCAATC TGTAGCAGTT CCCTAGGGCT GCCATGACAA ATTACTACAA 840
ACTTGGTTTC TTAAAACAGC AGGAAATTAT TCTCTCATGG CCCTGGAGGC CAAAAAGTCT 900
GGAATCAAGG TGTGGGCTAT GCTCCCTCTG GAGGCTTTAT TGAAGAATCC CTCCTTACCT 960
CTTCCAGCCT CTGGTGGCTC CAGGCAATCT TTGGCATTCC TTGGCTTGTG TCTGCGTCAC 1020
TCCAATCTTT GCCTCCATCT TCGCACGGCC CCCTCTTCTC CCTAAGTGTC CCTTCTCTGC 1080
GTTTCTCACA TAAGGACACT TGCTGTTGGA CCTAGGGCCC ACCTGGATCA GCCATGATGA 1140
CCTCATTTTG AGATCCTTAA CATAATTACA TCTGCAAAGA CTCACTTTCA AATAAGGTCA 1200
CACCCACGGG TTCGAGGAAG ACATGAATTT CGAGAGGTCA GTGTTCAACC CAGTTCTTGG 1260
GGATGTTCTT TTGTGTCAAA GTGCTTTCAA AGCTCTTGAA AATTCATGTT CAAATTCTCA 1320
AGTGCGAAGG GCTGATCTGT GAAGAGCAGT GCCAGTGTAT CCATAGCTGC CTGAAGGTGG 1380
ACGATGGGCA GTGCTGGGGC CAGGACACCT CCGGAATAGT GCTCCCTCCC 1430
|
