| Tag | Content |
|---|
EnhancerAtlas ID | HS091-12150 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr13:99426880-99429680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr13:99428796-99428811 | GAGGTCAGAAGTTCA | + | 6.38 | | RARA | MA0729.1 | chr13:99428796-99428814 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27651 | chr13:99427477-99429705 | Fetal_Intestine | | SE_28565 | chr13:99427274-99429851 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I098775 | chr13 | 99427743 | 99429621 |
|
Enhancer Sequence | TGCCACTGTA CTCTAGCCTG GGCGACAAGA GCAAAACTCC GTCTCAAGAA AAAAATAAAT 60
AAATAAAAAT AAAAACATGG AGAAGGCAAA GCACTCAGGC TTGGTTTTCT GCAGGTGGGA 120
AAGGACCACA CAGAGGCCAG ACCCCTTCAG ACGTGCCTGC TCCCCACACA GCCGGCTTGG 180
GAGCCAGGTG GCCATTTTCC CATGTGAAGG AGAATATTTC CCTCCTCATT CAGGGCATCT 240
GGGGTTGGGG GCCAGGACCT CCTCTGTCCC TGCTTCTCCT ACATCCATCT GTCCAATGGA 300
TGCCAAGCTT CGACTGGTTG CCAGGCATGG GGCTGGGCCC CAGGAGAACC GGAGCAAGGA 360
CGAGACCTCT TCTCCATCCT GGTGAAGCTC TGTTCCTGGG CGGGTTAGTC AGGTACTCAG 420
GACACCACAG AGGGCAGTGG GTGGAGGGCT TCAAAGTCAT GCCCTCGGTA ACTGGCCAGC 480
AAGTGTTGCC ACCAAGAGCC GTAAGGGGGC TTCAAAACGC TGGCACCTGC TACTGAAAGG 540
TTTGTGGAAT CTTCTTGAGA TTAAAAATGA AAATGCTGCT GGCCTCTGTC TCTACACATT 600
CTCTAGTGAC TCTGTGTCTT CATCAGGGCA AATCATTCCT TGCAATAAAT ATCTTGAAGG 660
TGTTCAATGA GCTGGCTAGT TAGAGCTTCT CTGGAGCCCT GTGTTCGAGT GGGACACTTG 720
ACTTTTGCTG TCAGGCCCCT CTTGGCATTG GGGTCACAGG GAGCAGTGAT TCTCACACCC 780
TACTGTGCAA AGGAATCCCC TGGGGCTTGT TGGAATGCAG ACTTGCGCTC GGTGGCTCTG 840
GGTGTGGACG AGGACCCTCT GCCCGCAAGC TCCCAAGTAC TTGTCTGTTC GCGGCTGCTG 900
GGCTGCAGGT CACCCCTTGA CCAACAAGAG CTTAGACGGA GGCTTCTCCG CCGTGGCTGT 960
ACTGCTGTCC TGGACGATCT CTGTCTGTTG TGGGGGCTGT CCCGTGCACT GTGACATGTT 1020
CAGCAGCATC CCAGCCCTCC ACCCACAGGG TTACAGTAGC ACCCCCACCC TCAACCATGA 1080
CAACCAAAAA TGTCCGCAGA CGTTTTCGTT TGCATCCCCT GGTGGACTGG GGCATGGGGG 1140
CGGGGTGTTG AGAACCACCG ATTAGTAGAC TTTCAAAGAC TCTCCCAAAT CCAGTTTTTT 1200
TGTGATCAAA AGTCCACATC AAATCCTCTT AGTTGGAAAA CACGCATCAC TCTAAGGCTG 1260
AAAAAGATGA CTCCACAGCT GAGCTCTAAA TGTCCTCTTA AAAATATAAA ATCCCAGATC 1320
AACCTGTCTT CACAATGGCC GCATGTAGCA GCCCCTCCAC AAAGACTGGG TACAGTGGCA 1380
TTTGCACCTT CTAAGGGACC CTGGAGTGCG GCCTGACTGA GAGAGTGGAT GGGGAGGGGA 1440
TGCCGGGTCT CTGGCTCAGG TGTTGCGTGT TGGGAGCCCA CTAGGTAGAA CAAGTGTCCT 1500
CCACCCAGCT CAGCTCCGGA GCCTTCCTCG AAAGGCAAGA GGTCAATTCA TCTTCTGCCT 1560
CAGCAGAATC GTCCCTTCCT TTACAAGGGG ACTTTGCTCC ATGATCTGAC AGACCTGGGA 1620
AGTGTGTGGA GGTTTTACAC GATGACTCAG TGCACATCAG AGTCAGAGAC AGGACGGCCG 1680
AACACTGATT CCAGAGATAG GCATGTGGGC CCCGCCCGGG AAGGAGAGCT GCCTGGGAGA 1740
TGGGGAGCTG CAAGAGAGCA CCCAGAGGGG TAAATTTGCA CAAGGCCACT GCGTACACTG 1800
GTACGTGCTT CCTTGAAAAT GTGACATTTT CAGGCAGGGC GCGGTGGCTC AAGGCCGGGC 1860
ACGGTGGCTC ACGCCTATAA TCCCAGCACT TTGGGAGGCC AAGGCGGATG GATCACGAGG 1920
TCAGAAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC CATCTCTACT AAAAATACAA 1980
AAATTAGCGG GGCGTGGTGG TGCATGCCTG TAATCCCAGC TACTTGGGAG GCTGAAGCAG 2040
GAGAATCGCT TGAACTCAGG AGGTGGAGGT TGCAGGGAGC CGAGACCGTG CCACTGCACT 2100
CCAGCCTGGC AACAGAGTGA GACTCAGTCT CAAAAAAAAA AAAAAAAAGA AAATGTGACA 2160
TTAGTTTTCA TTGCTCTGAA AGAAAAGCGA GACTGTTTCA ACAGTTGGGT AAATTACTGT 2220
GCTTCCAGTA ACAAAGACAG GTTTTCAGAT GCAAAGTGAC ATGTACAACT ACTGTGGAGA 2280
AATGTCCATC AGACGGAGTG CTAAGTGGGG ACAGTGTGCC ACCACTGAGC CAAGAATGGA 2340
GGAGATGAAT GTGTGTGTGA TATGGAAAAT AAATGGAAGG AGAATTCAAA ACCTTTCAAA 2400
TTTGTTTTAT ATAAGGAGTA GAGAAGAATA ATGAAAACAA GCACAAAAGT TAGACTTTTT 2460
TTTTCTTTTT TGAGACAGGC TCTTGCTCTG TAGCCCAGGC TGGAGTGCAA TGGCACAATC 2520
ACAGATTACC GTAGCCTCCA CCTCCCAGCT CAATTGATCC TCCCACCTCA GCCTCCTGAG 2580
TAACTGGGAC TACAGGCACA CATCACCTCA CTTGGCTAAT TTTTGTATTT TTTGGAGAGA 2640
TGGGGGTTTT GCCATGTTGC CCAGGCTGGT CTCAAACTCC TGGGCTCAAG CAATCCTCCT 2700
GCCTGAGCCT CTCAAAGTGC TGAGATTACA GCTGTGAGCC ACCACACCCA GCCTAGACTT 2760
TTTTACATCT GTTTTCTCGC ATAATTGGCT TTGGAGTCAT 2800
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