| Tag | Content |
|---|
EnhancerAtlas ID | HS001-06605 |
Organism | Homo sapiens |
Tissue/cell | 786-O |
Coordinate | chr4:153890910-153893520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PPARG | MA0066.1 | chr4:153893014-153893034 | TGGGGGTGACCCTGACCCTC | - | 6.1 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28188 | chr4:153890946-153892181 | Fetal_Intestine | | SE_28967 | chr4:153891032-153892202 | Fetal_Intestine_Large | | SE_36704 | chr4:153890944-153892733 | HMEC |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH04I152969 | chr4 | 153890840 | 153892846 | | GH04I152972 | chr4 | 153893343 | 153895742 |
|
Enhancer Sequence | TCCTGGGTTC AGGTGAGTCT CCTCCCTCAG CCTCCTGAGC AGCTGAGACT ACAGGCGCAT 60
GTCACCACAC CAGGCTAATT TTTTGTATTT TTAGTAGCGA TGGGGTTTCA CCGTGTTAGC 120
CAGGATGGTC TCAATCTCCT GACCTCGTGA TCCGCCCACC TCCCAAAGTG CTGGGATTGT 180
AGGCATGAGC CACTGCGCCA ACCCAGTCAT TTTTATCTCT ATAAGTAAAA CGTTTCATAC 240
AGCTGCATAC TTTTCTTTCT TAAATTCAAC TTCCTTTTGA ATAGGTGAGA TAAAATTTTT 300
CGAGGTAGGT CAGGGTCAGG GCACTCAGGT CTCTGAACAC CAGTCTGAAT GCTGGACTCA 360
AACTCTATGC CATAAGAAGT GGGGAACTCT TCAAGGATTC AGAGCAGAAA AATAACAGGA 420
ACACATTTTT GCAGATCTAT TTCAGCATTT TCACCCTTGG GGTAAGAAAT ACTGAGTAAA 480
CTTGTTTGAA ACTTCAGTGT GTAGCAGGCA AGTTAGAGAT GTAAGGTTGA CTTGGACACT 540
ACAGCTGCTA ACCTGTTGAC ATTCTTGCTT TGCCAGTGTA GCTTTGAACT TTTCCATTTC 600
TGGCCCTAAT CATGTAGAAC TCCTGCCCGG TAACTTCAAG TGTGGTTACT GTTCAGATCC 660
ACATTCAGAA TGTTTCATTT TCCCAAGTCC AAAGGGTGAC TTCAGTGTGT TTAAGATTTT 720
CCTTCCTGGT ACTCTGTCAA TCCCCACAGG ATCTAGAGAT GAAACATACG AGGTGGAGCT 780
GAGCTCCCAT GTAGATTCTT GTCAAGAGGC CTATTTTTCT GCAGTTGAGC TGTTCTTGGC 840
TGGAATCCAT CTTTCCCCCT GTGGAAGAAT GACAGGCAAA GATTTATCCT TTCATTAATA 900
CCATTCCTCC ATAAAGAAAA ATACAGCATG AATGCACACA CTGCCTTGGG CTACTGACTC 960
AGGTGGTTAC TTTCTCTGGT ATTTGGTTTC CTACATAGTT TTCGTTTCTT ACTACCTCTT 1020
GAGTGTGTTT GGTTTAAGAG AAGGGCTTTT AAGGGGGAAA GTGGGTTGGA GTGGGTAATA 1080
GGTGGCGTCT TCACAGAATT TCCCTGTAGG TTCTGTAGCT CTCCACACAG GTTCAAACAG 1140
CAGTTCTACC CCTCCAAAGT GGGCAACTTT AGCTTTACCA TTTCCCAGCC CATCCCCACT 1200
TCACTCAAAA AATGTTTTCA AATATAACCT TTTTTAAAAA CATGATACAT GTGATTTCAT 1260
AAAGTAACAT ACTTCATTCA TTCCTTCTTC ATATAACCAT TATTTCCCAG TAAACAAGGA 1320
AGCAACATAG GCTAGGCTCA GTGGCTTACC CCTGTAATCC CAGCACTTAG GGAGGCTGAG 1380
GTGGGAGGAT GGCGTGAGGC CTTCCTGGGA AACATAGGGA AACCCTGTCT CTACAAAATA 1440
TTTAAATATT AACTGGGTGT AGTGGTGCAT AGCTATAGTC CCTGCTACTC AGGAGGCCGA 1500
GGTGGGAGGA TTGCTTGAGC CCAGGAGGTC AAGGGTGCAG TGAGCCATGA TCACACCATT 1560
GTACTCCAGC CTGGGTAATG GAGTGAGACC CTGCAGGTCT CAACATAAGA CTTCAGTGTG 1620
ATTCCAAATG TTCATTCTCA TGGGCTGTGG CTGCTGTGGA GCCCTTTTTC TCCGCACCAT 1680
ACTGCTTCCT CATGCAGCTC CCCATGTTGT CACTGAACTG CCATCGGGGA AGTGTGTGTG 1740
ACCCTTGGAC ATGGCAGATT CCATGCTGAA GGCCTTGGAA ATCATTGGAG GAAAACAAGC 1800
TTCCTTTCTT CCCATCTCTG TGTTGAGGCA GTACCAGAAT GCACAGGGGC CTCAGAGACT 1860
TATTTGTCCT AGAAGAATTA GGAGAAAATG AAGAAGCAAA GAGGGTGGTT TTGTAAAGGA 1920
CAGTAATGCC TAGCCATTGG GACCCATCAG AATCTCCTGG GGTGGTGCTT TCAGAAAATA 1980
TTAGTGTTGG GTCCACCCCA AACCTGTGAA ATCGAACGGG AGGAATACAG GCATGGCCTG 2040
TTGCCAAGCT TCCCAGCTGA CTTGGATCAG CACCCCGGGT TTAGGCACGA GGGTTTTGGT 2100
CCTGTGGGGG TGACCCTGAC CCTCACAGAG CTCATTTGGG ATTAAGCTTA GACACCCTCT 2160
CAGTGGGGCA AAATTGATAA TGCATCAGTA GAGCGAGTAG CTTCAGGGAC CCTAAAGTAA 2220
ACTCTTGACC AGTGTAAGAC TCAATTTTAA GAGGAAGAAG AACAGATGCA AAATGGATCT 2280
TCCTTGGTAA AAACCAGTTG TATACCTGTG TAATTTTTTT CAGTGACATT AAAAGTGAAC 2340
ATTTTGTTAG TGACGTTCTG CAGGTTAAAG TTCTTAAATC TATCTTGTTG CTTAGTCTAG 2400
GTCTCACACG GGACTTCACC TTGCTTTCCC CGAGGTTTGT TCTGGGTTGA ATTATTTTCC 2460
TTTTGGCTCT GATTGCATTG GCCTTGCAAT AAACCTTCCT TTTCCAAGAC CTGAAATGAA 2520
ACCCCAGAGC ACGTCTTCTC TGGGCACCGG ATGCAGTGCC CAGCGCCGCC TCAGCTGACA 2580
ACGTTTACCT CAGTGTGTGT TCGTTTGTTT 2610
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