| Tag | Content |
|---|
EnhancerAtlas ID | HS118-16048 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr6:36584020-36585750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr6:36584033-36584051 | CCTTGACCTTATGATCTG | - | 6.32 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28352 | chr6:36584242-36585491 | Fetal_Intestine | | SE_29430 | chr6:36584342-36585616 | Fetal_Intestine_Large | | SE_52665 | chr6:36584362-36585875 | Small_Intestine | | SE_65091 | chr6:36584389-36585276 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I036616 | chr6 | 36584348 | 36585853 |
|
Enhancer Sequence | ATGGTCTCGA TCTCCTTGAC CTTATGATCT GCCTGCCTTG GCCTCCCAAA GTGCTGGAAT 60
TACAAGCGTG AGCCACTGCG CCCGGCCAAT TTTTGCTTTT TTAGTACAGA CAGGGTTTCA 120
CCATGTTGGC CAGGCTGGTC GGGAACTCCT GACCTCAGGT GATCTGCCTG TCTCGGCCTC 180
CTAAAGTGTT GGGATTACAG GCGTGAGCCA CCATGCCCAG CCAGGGATGG TGATTTTCAA 240
ACTTTAAACA TAGTTAAAGT TTTTGGAATG AAATCTTATG TAGAATACAG AAAACAGCTA 300
AAAATGGTAT AGCTATAAAA AGTATAGGTT CTAATAATAT TGGCTCATAA AGACAAGAGA 360
AATCCAATTT CCTTCTGTTA TTTTGGTTGA ATAGAGAAGT GCAAATGGTA ACATTTTTTA 420
ACACTTTATT TTGCAATCCC CGAGGTGACA GGATAGGAAG GTCCATCCCA TAAACAACCT 480
AGAAGCACAG ACGTCAGAAG AACATCACCC CAACATGTTT ATAGGCATTT GGTTGAATAG 540
GTTTTATGTG GGGGAAAAAA CAGAAAACTT AAAAATTGTT AGACCTGTAT ATATTTTCAA 600
CTCAACCAAG TGCCTGTGAG CCCTCTGCAG CCATAGTGGG AAAAGTCCTT ATACTGCCCA 660
CACCTTCATG CTACAGATGA AGAGCCTGAG GCCCAGGGAG GAGGAGGGGG TGGCTGAGAC 720
TCAGGGAGCC TAGGGGGGCC ATCTCCAGGG GCTCGGCCTC CTGCCACCCC ATCCGGTGCC 780
CTTTCTGAGT GACCAGTCAT GACATCTGGT ATGGCAGTGT GCTGGAGCCT GGCTGTTCAA 840
CCCCTCACCC TGAGAGGGCT CTGGCCACTT GCCCATCTCC CTGGCAGATA AAGCCTCAGA 900
CAGATGGCAA ACAGTACTTG GCTCCAGGAA TCAATTCAGG TCTGATTCAC CAGTGGTTTG 960
TGCCCGAGCC AGCGCCACAG GCTGTCTCCT TTCCCCTGTT CTATCACTCA CTACCCTCAC 1020
TGTGGCCAGG TTGGGACTCT TGAGCAACAG GCAGATACCT GTGATCTTGA GAATTGCACT 1080
GACTCTTTTG AGGGTTTTCC AGGCCACAGC AGGACTTGTC TGCCTCATTC CTCTGGGCAG 1140
CTCAGAGCAT TACCCCATCA GCTGCAGTTT CAGTATCAGG GTGGGGCAGT GGTGTGGGGT 1200
GGGGCACCGT GTTACTAGGA CTAGCCCTGT TGGCTGCAGA CACATTGGCA ACAGGTGGTG 1260
GCTCAGGGGC ACAGAACAGG TGGACTACAC ATCTCCAGGA TGAAGTGTCA TTTATTGGCA 1320
TTTGCCTTTT GAAAGAAGCA ATCTACTTAT AAATGGCAGG ACCCTTTTTA TTTTCTTTTT 1380
TGAGAAAAGC ATTTTATTAA ATCCATATTT GGAGATATGT TTTAGCAAAG TATAATTAGC 1440
ATTTTTTGTT TAGAGGATGA ATTGTGTTGC TACTCAATAG AAGGAGAATA TGGCATACAA 1500
ACAATGCTTT TATGCAGAAA CATGTGTTTT TGTTTTTGAG ACAGAGTCTT GCTCTGTTGC 1560
CCAGGCTGGA GTGCAGTGGC GCAATCTCGG CTCACCTCTG CCTCCTGGGT TCAAGTGATC 1620
CTCCTGCCTT AGTCTCTCAA GTAGCTGGGA CTACAGGCAT GTGCCACCAC GCCCAATTTT 1680
TGTATTTTTA GTAGAGAGGG TTTTGACATG TTGCCCGGGC TGGTCTCGAA 1730
|
