| Tag | Content |
|---|
EnhancerAtlas ID | HS127-00101 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr1:8242310-8243750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr1:8242600-8242611 | TTTGTTTACTT | - | 6.62 | | IRF2 | MA0051.1 | chr1:8242750-8242768 | AGAAAGCGAAAGCATTCA | + | 6.14 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_33918 | chr1:8241396-8243905 | HCC1954 | | SE_34231 | chr1:8240249-8246041 | HCT-116 | | SE_34786 | chr1:8240946-8245641 | HeLa | | SE_47106 | chr1:8240454-8246507 | Panc1 | | SE_65889 | chr1:8242598-8243711 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I008180 | chr1 | 8240803 | 8245776 |
|
Enhancer Sequence | GCTCTCCCTC CTCTTTCTAG GGCTGCGGCC TTGGTGATGT CAAGAACATT TTGTAAATAT 60
TACAAGTAAG ATAAGGCATT GTGACTATTA CTCGTTAAAA TCACTTTGTT TCCTGACTTA 120
GGTGATTCAC TGCAACCCAG AGAAAGTTTT GTGTTGTGTT CTGGCTGGCG AAACTTCTGC 180
AAACAACGAA TGCTTCTTTT CATCAGCCTA TTCTGCGTTG GTTGGTAGGA TGTCAGTCTA 240
TAACCACATC AATTTCAGGT AATAACAAGT GTGTGAGCTT TCTGAAGCTT TTTGTTTACT 300
TATTTGTTTT AGGGTTGTTC AAGTGTGACT CATGTAGTAG CACTGCATTC TTGAGAATTC 360
ACAGAGATCG AAACACAGAT ATGAAACAGG GCCAGAAAGA ATAAGGCGTT CCCAATATAT 420
GAGAGTAAAA AAAAAGCACA AGAAAGCGAA AGCATTCAAT GTCTGCATCC TGTATAGATG 480
AGAAACTTAG CAGTATCCTC TTTTCTTTTT GGACCAATCA TATGCTGATA AAACAGGGTC 540
TCGCTGCTTT CCCCCCATTT TTAACATCTT CAAACATTCT GAGAGCCTAC GGGAATAGAG 600
GCAAACAGGT TTGATGTGAC TGGTCATTTG GCCAAAGGTA TTTTACTCTG CGCTCAGCAT 660
TTTGTTTCGT TCATGCTCTC TAGCAGTTTG GAATCTAAAA AGGAAAGATT AGATAGAGGA 720
AGTGTGAAAA TGCATACGCA ATGTGGGAAA CCAGGCCATG AACTTGAGTT TTTAAATGCA 780
TGGTATAAGG CCGGGCTCAG TGGCTCACGC CTGTAATCCC AGTACTTTGG GAGGCCGAGG 840
TGGGCGGATC ACCTGAGGTC AGGAGTTCGA GACCAGCCTG TCCAACATGG TGAAACCCCG 900
TCTCTACTAA AAATACAAAA ATTAGCCGGG CATGGTGGCA GGCGCCTGTA ATCCCAGCTA 960
CTCGTGAGGC TGAGACAGGA GAATCGCTTG AACCTGGGAG GCAGAGGTTG CAGTGAGCCG 1020
AGATCGTGCC ATTGCACTCC AGCTTGGGGG ACAAGAGCAA GACTTCGTCT CAAATAAATA 1080
AATAAATAAG TGCATGGTAT GGTTTGGCTA AGTTGGAAAC CATGGGATAA TCTGGAATGG 1140
TTTATTAGAG AGGCTAATGG TGGGGAGGTA GGTACCCAGA ACCTTGGGCT AGAGATGACT 1200
GACCCTTTCT GGCTGTGTGA TCTTGGGCAA ACTGCTTCAC TTCTCTGTGC CTCAATGTCC 1260
TCCATCATGA AGAGAGAATA TAGGGTGCCT TCATTGTAGG GTAGTTGTAA GGATGAAAGG 1320
AGTTGGTATA TATAAAGTAC CTATCTCAGT CTAGGGCTTC TCAGCCAGCA TGCAGGGTAT 1380
ATGGGCTTCA AATGGATGAA AAAGGTGCTG ATCCCAGGTA CCTGGCTGTG AGCATCCTCA 1440
|
