| Tag | Content |
|---|
EnhancerAtlas ID | HS118-04790 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:106214010-106215380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr12:106215069-106215080 | TTTTATTGCTT | - | 6.32 | | MEF2C | MA0497.1 | chr12:106214778-106214793 | TGCTATTTTTGTAAA | - | 6.13 | | NR3C1 | MA0113.3 | chr12:106214402-106214419 | AAGGACATTGTGTTCTG | - | 6.06 | | NR3C1 | MA0113.3 | chr12:106214402-106214419 | AAGGACATTGTGTTCTG | + | 6.08 | | NR3C2 | MA0727.1 | chr12:106214402-106214419 | AAGGACATTGTGTTCTG | - | 6.3 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I105820 | chr12 | 106213956 | 106215826 |
|
Enhancer Sequence | GAGAAGAAGA ATGTTTCTAT TAAAGTGAAG CCCAGGATGG CAGTGTTTAT GTGACTTGAG 60
TTCTTGGCTA AAGCTGTGTT AGCAAGTGTA CATCCTGTGT ACAGAGAGGA AGGTGTGTGT 120
GGACTTTAAA CCATTCCCCA GGTATGGTTC CATGGCTTTT CCAGCCTAGC TCATTCTTAT 180
TTCTTTCTCC CTCTTGTCCT CACTCTTGGC AGTTTCTTCT CTGGTGGCCT GCTAAGAGTT 240
ACAAGTTCAT TAGCAGCATC AACTCAAAGA GAGATCAAAT CTGTGGAGAC CCTTGCTCTT 300
TGAGCACCTT GCCTGCAGCC CTTAAGCTGA CATGCACTGC AGATGGCCCG AGCTGGGTGG 360
AGGGCATACT GTACAGAAGG AGGATACAAG CCAAGGACAT TGTGTTCTGT CTCTAATCAA 420
ACCCCATTAA GTGGCAAATT CCTCTATTCA AAAGTTTTCA TAGGATGGTA CTTTCAAAAG 480
AACTCCAGCT GGTTAAACTT AGGGCCTGAA ATAAATCCAG TCTAATAATT CGATCTGGCT 540
CTGGGCCTGC CACATCCTTT CGATGGAAGA ACTCAATGCA TTTTCATTCA TTAGGGGCCT 600
CCTCTCAATG TTGACTCAGA GGTAGGCCAC AAAATTCTTT GCTTGTGTTG GCCTTGAGAG 660
GACTGGGTCA CTTAATGAAA CAAGTAGCTT CCAGTGTGTC CCTGGCTGTT AACGCAACCT 720
CCTCATGCTT GCTGGTGCAT TTTCAGAGCT TGATTGTGCA AGAAATATTG CTATTTTTGT 780
AAATGGTTTG GCCTCTGCAG TCATTAACCT GGCATTTCTC CCCCGTGGAG GGGAAACATC 840
ATGTGTCCAT TGATTCCTTC TTTTGTTTGT AAGCTGTTTG CAAAAGAAAG CCCTCAAAAA 900
AAGTCCTTTC TCCCTGCATC TTGTCATTAG TACCAACATG GAATTTCTTC TAGTTACTTT 960
TATCAACTTA CTAAGTAATA TTTTTCAGAA TATTTAGCAG TATTTTCCTG GTTCTTTCAA 1020
GTCTCTTGGC TGCTGGAGTA CATCGCTAGT CCTTGATCCT TTTATTGCTT AGTTCCATTC 1080
ACAATTACAA GTCAGCAAAT GTTTCAGAAA TGCCTTCAGT GGGCAGAGAC TCTGCCAGGT 1140
ACTTGGGGTG AAGGGAGGTA GAAAGAAATT TCCAATTTCA CAGATTAAAA AGTTGACCAC 1200
ACCAAGCCCT TCCTCCACTC CTCTAGGCTG AATCCTTGGC CCCCTCCTAC ACTTGTACCT 1260
TGATTATGAT CCTTAGTGAT CTCCTTCTAG GAGCTGGGTA TGGCAGGCTT TCCATGTAGT 1320
AATCTCAAGC CTCCCAACTT AACAGCAAAA TAGTACATTT TGATGCCATG 1370
|
