| Tag | Content |
|---|
EnhancerAtlas ID | HS179-03129 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:212090530-212092140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr1:212090805-212090816 | TGATTGAATTA | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27820 | chr1:212088149-212095215 | Fetal_Intestine | | SE_28649 | chr1:212087848-212099385 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I211914 | chr1 | 212088252 | 212094992 |
|
Enhancer Sequence | TGTATAGATG AGGAAACCAA GGAACAGTGA AGTCAAGCAA CTTTCCCAAG GTCATTACCA 60
GAACAAGAAA GGAAGACACC TTCTACAAGG AAAGAGTATA CAGATGGTAC ATTTTAGGAA 120
GGGCACGGCC TGTGGAAGGT GCTAATTTCT AGATGCTACT TTAGAGTATG ACTTTGATTG 180
ATTACTTGCA AAAGTAGACC TATGCTTGTT AGTTATGCCT CTTTCACCTG CTACTCCTCC 240
ACAGTTGGTC AAGACCAAGC CCTAGTCATC CTTATTGATT GAATTAGGAG CAAAATCTAG 300
GTTCTAGTCC TCCTAATTCT ACTACTTACA AGTTGCCTCA CCTTAGGAAC GCCATTTAAC 360
TGCTGTCTCC TTATTTTCCC AGTCTGGCCT TGTCCTCACC GTTGTGGGGT ATCAGGCAAG 420
ATAAAGCACA CAAAGTCTCT CTGCATGCCG GAGAGCATTT TGCAGCATGA GGAGATGTTT 480
TCTGCCCCAC CTATGTACTA GAATCCTCCA AGGAGCCCGT AATGTGAGTG TAGGGGTCAG 540
GGGCAGGCTG GTGACTGGAT GCTTTTGTTT AAGTTCCACC AGTGATTTTG ATGCACATCC 600
AAATGTGGAA ACCACTGACA AAGTACAAAA GACAAACAGG AGAAGAGAAA TAAATTGTGA 660
GCTAAAGATG CAGGCATGTT TTAAGCTCTC TTTAGAGTGG ATAACTAAGG GCCAACTTAG 720
AGAACAATTA AATTGCCCAT CTTTTTCAAG GTACCTGAAA CCCTAATCTC AAGTCCCTTT 780
TTTCTTCCTG GAAAAGATGT ATATGACTTC AATTACATTA CTTTTCTTAC CTAGCAATCT 840
AAACACACAC TGAAGATTTC ACACGCACAC ACACACACAC ACACACACAC ACACACACAC 900
ACTTCGTGAA TCATCTCTGC CTGGTTGCAT GCTGAAGTCA GATTCCGAGT AATGTCTGTT 960
ATTCTTTAAC CTCTGAGTAA TCACTCTGGC CCTGGTCTGC TCTTTATCGT CCAGGAAAAC 1020
AATCTGATCA AGCCTTGGAT GATGGATTCA TAGTTGCTCA AGTCTCCAGA GTGCTGTATA 1080
AACCAGACTA TTAATTTATT CCATGGGGAT ATTCTGTGAA AGTCCTACTT CTCCTTTTTA 1140
ATAATTGAGT GGCCTCGAGC AAGTCACTCA ATCTCTCTAG GTCTCTAAGA TGATTATGAT 1200
CACTAAGCAT CACTCTTTAC AAAGTATTTC CTTCTTTGTG ACATCTCTCT TTAAAATGTC 1260
AGTTGAATGT TCTCAGAAAC TTGTTGCAGT GGGCATAACA TTAAAGAAAA TGGGTAAGAA 1320
TGAGAACAAT GAATTTAAGG AACATTTCAT TCAGTCCATG GGACACCAGA GTGGACAGCT 1380
GTGACTTGTG TCTGCTCAGC ACTTCTTCTG CTCTTCAGGG GACAGAACTT CCTTCCATGG 1440
GGGAACTGCT CCTTTCTTCT TCCACCTGGT TGTGAGGAGG CTGCTGATCA AAGGACCCTG 1500
GCCTCCTCTT CTTCGGCCAC AGGGGTGGGC ATGTGACCCT GATTCAACCG TAATAACAAC 1560
CTACTCACCT AGCCACAGTG ATTGATCTGG GAATTCATCC AAGGATCAAT 1610
|
