| Tag | Content |
|---|
EnhancerAtlas ID | HS091-16357 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:11918600-11920980 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr16:11919480-11919491 | TGCTGAGATTT | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr16:11919437-11919452 | TGATCTCTTGACCTC | - | 7.23 | | PHOX2A | MA0713.1 | chr16:11918622-11918633 | TAATTGGATTA | - | 6.02 | | Phox2b | MA0681.1 | chr16:11918622-11918633 | TAATTGGATTA | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09876 | chr16:11917177-11919169 | CD14 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I011822 | chr16 | 11916063 | 11919199 | | GH16I011825 | chr16 | 11919481 | 11919630 |
|
Enhancer Sequence | GGAAAAAGGC TTGGCTTCTA ATTAATTGGA TTAATAGCCA ACTTCCAAAT CAATTGTTTT 60
TCTTAATGCA CTGGCAAAAG TCATTTACGG AGTGAAAACC TGAGAACATC TACTATTCAA 120
TCATCTTTCC TGAAGAGATA AGTGGTAAGA GTAACTCTGC CCAACATAGT ATGAAGTCTT 180
AGGTTTTTCA AGCAGTAAAT GAATACTGAA TGAAAGCTAA GCATAAAGAT AATACATTAA 240
TGGCCGGGCG TGGTGGCTCA TGCCTGTAAT CCCAGCACTT TGGGAGGCCG AGGTGGGCGG 300
ATCACCTGAG GCGAGGAGTT CGAGACCATC CTGTCCAACA TGGTGAAACC CCATTTCTAC 360
TAAAAATACA AAAATAAAAA TAGCCAGGCA TGGTGGCGCA TGCCTGTAAT CCCAGCTACT 420
CAGGAGGCTG AGGCAGGAGA ATCGCTTGAA CACTGGAGGC AGAAGTTACA GTGAGCCGAG 480
ATCACACCGC TGCATTCCAG CTTGGGCAAC AAGAGTAAAA CTCTGTCTCA AAAAAAATAA 540
AATAATACTA CATTAATATA AAATCATGTG GACAACTGGA GTGAAAAAAA ATTCAAAGAG 600
AAAAAATGGT AAAACCTTGC TTTTTTTCTT TTTTTTTGGG ACGGAGTCTC ACTCTGTCGC 660
CAGTCTGGAG TGCAGTGGTG TGATCTCAGC TCACTGCAAT CTCTACCTCC TGGGTTCAAG 720
TGATTCTCCT GCCTCAACCT CCCGAGTAGC TGGGACTACA GGCATGTGCC ACCACGCCTG 780
GGTAACTTTT GTATTTTTAA TAGAGACAGG GTTTCACCAT GTTGGCCAGG ATGGTCTTGA 840
TCTCTTGACC TCGTGATCTG CCCGCCTCGG CCTTCCAAAG TGCTGAGATT TCAGGCGTGA 900
GCCACCGCGC CCAACCGGTT TTTTTGTTTT GTTTTGTTTT TGAGACAGGG TCTTGCTCTG 960
TTCCCCAGGC TGGAGTGCAG TGGCGCAATG TCAGCTCACT GCAACTGCTG CCTCCCAGAC 1020
TCAAGTGATC CTCCCACCTC AGCCTCCCAC GTAGCTGGGA CTACAGGCGC CTGCCACCAC 1080
CCATGGCTTA TTTTTTTTGT ATGTTTTTGT AGAGACGGGG TTTCACCTTG TTGCCCAAGC 1140
TGGTCTCAAA CTTCTAGGGT CAGGCAATCC TCCTGCCTCG GCCTCCTAAA CTGCTGGGAT 1200
TACAGGTGTG AGCCACCACA TGTGGCCCAG GTGTTTTCTT TAAGTGGGTG ATGGTGACGA 1260
TCAACTCCCT TAGGTATTTA GAGTCCAACA GATGTATTTG AGAATGGAAT AGTTTTAGTT 1320
TCAAAGATCA CTATTTACAC AATGGCAAGT AATTATGTCT TTGCAACTGT ATACACTAAA 1380
CATTTTAGGT GTCAGGTTAA ATACTAGGTG GAACAGAATT TGTCACAAAA TTTTACAGTA 1440
TGTAGGAACA AAAAAAACAC TAATGAAAAC AATGACAAAT ATTGGCCTTT TAGGTTTGAA 1500
CTCACCGTTA ATGGCACCAT TTTATTAATT TGCCATTTCA TATGATGTTT TAACCCTAAA 1560
TTGCTGGTAA GTTTTGTAGC TGAATTTTCT TAGCATTTCT GGCTAACTAT GCTGTGTTCT 1620
TTAGTTTACT AACAATTTTT GTTTCTGATT CCCTAATGTT TAGCCATCCT TACATTCCTC 1680
AGATAAGCTC TCCTAAGCTG TTATTATCCT GGTTAAGCAG TATGTGGTAT CTTACATTTA 1740
TCTTAAGACC AGGTGATAGG AGTTTTTCTG GCGAAGAAAA CTACTAGGTT TGAGTACCGA 1800
AAAAATTACT TTCGCAGAAT GAATTGGGAA TCTTTGAATT ATAATGGCAA CAACTCAAGA 1860
TTTGTATGCA TGATATTATT TTATTTTTCG AGATAGGATC TTGCTTGCTC TGTTATCCAG 1920
GCTGGCAGTG CATTGGCGTG GTCTCGGCCC ACTGCAACCT CCGCCTTCCA CACTCAAGTG 1980
ATCCTCCTCC CTCAGCCTCC AGAGTGACTG AGACTAAGCC ACCTTGCCCA GCTAATTTTT 2040
GTATTTTTAG TACACACGGG GTTTGCCACG TTACCCAGGC TGGTCTGAGC TCAGGGGATC 2100
CACCCACATC AGCCGTCCAA AGTGCTAGGA CTATAGATGT GAGCCAGCGC ACCTGGCCCA 2160
CAATATTAAG TGAAATCTCA CTGTCTTTTC TCTTCCAGTT TTTAGGTTTT TGTCTCTTCA 2220
TTCAGTTTTG GGAACTTATT AGTTCCCATT ATCTAGACTT AAGAATGTTG TATGGGCCGG 2280
GCGCGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGCGGG CGGATCACGA 2340
GGTCAGGAGA TCGAGACCAT CCTGGCTAAC ACGGTGAAAC 2380
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