| Tag | Content |
|---|
EnhancerAtlas ID | HS060-02792 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr1:206939580-206940940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:206939770-206939784 | TCGCTTTGATGTTT | - | 6.54 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_18640 | chr1:206938558-206940480 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19631 | chr1:206939257-206940450 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_61266 | chr1:206939355-206991151 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I206765 | chr1 | 206939241 | 206940345 |
|
Enhancer Sequence | CCCTGAGTAG TTCCCAGCTT GACTTTTCCC TTTAGCTTGG TGATTTTGAG GCCCCAAGAT 60
TTTCCTTTCA CAGACTCAGG ATGTCTTCTT CAGTTCAGGA TGGACAGCCT CAGAGTAGAG 120
AGCTTCAGGC CCCCTCTCCT TATCTTCTGC TAACCTCCAT TCTTACTCCT ACCCTTTCAT 180
CTCAGAATTT TCGCTTTGAT GTTTCCCACT TCCTTCCTAT GGTTACTTTA ACCGAAGTGA 240
GTCAGGTCTT ACTGAAAAAC TGACCACAGC CTGTCCGCTC CCAGCCTTCC CCAGACCAGG 300
GCTGCCCAGG CAGAGCGTGA GGGGGACTAG TGTTTACTCA GCTCATTTTT TTCCTCCTCT 360
CTCCTCTAAG TCACGGGGCT TTGAGTAGGG CTTCCCCAGC CACCGTGCCC CTCCCAGCAG 420
ACCGCAGTCA GAAGCCAATC TCACATTTGT CTGGTGGCTC AGAGAGGGGA CAGAAAGAGC 480
AGCAGCTTAT GTCCTTGGCT ATCCTCTCAA GTGGGCTAAT TTGCTTATTT TCAACTCTGT 540
TGGGTCCAGC CCTGTTGCCT CTGATCTCAG CTCAAAGAGG ATTTGGCGGG AGTTTTTGGT 600
TGTGATAACC AATAACAACC AACTATACGC ACTGCGAACA TCTCCTAGTG CCAGAAGCCC 660
TGTTAGCTCA TTATCTTAAT CCTCAGGATA ACCCAGGCAA TTTGTATTCA CCCTAAAAAC 720
TTCCCCTGGC CGGGTGTGGT GGCTCACGCC TGTAATCCCA GCAATTTGGG AGACTGAGGC 780
AGGCGGATCA CTTGAGGCCA GGAGTTCCTA ACCAGCCTGG CCAACATGGT GAAACCCCAT 840
CTGTACTAAA AATGCAAAAA ATTAGCCGGG CGTGGTGGCA CATGCCTGTA GTCCCAGCTA 900
CTTGGGAGGC TGAGGCAGGA GAATCACTTG AACCTGGGAG GCGGAGGTTG CAGTGAGCTG 960
AGATCATGCC ATTGCACTCC AGCCTGGAGA CAGGGCGAGA CTCCGTCTCG AAAAGCAACA 1020
ACAAAAACAA AAACAACCTC CAAAAAACCT TCCCCTGTTT ACCTTTCTAA TTTTGGTACC 1080
TACAGAATCT CCCCGTTAGC CTTGAAAATC AGCATGATCT TTAAGGATTT AGGAGCAAAT 1140
CTTTAAAGGA TTGAGTTGTG GGAAGACCAT GATGTCTTTG CTACTGGCTT TTGCAGTGAG 1200
AATAGCTTTT TCTCTGATCA GGTTTGGAGC CTTCCCTCTC TCCTGGGGGT AGGGGGTAGC 1260
TGGCTTCCTT TCTCTGAAAT GCAGAATTCA TTCACCCACT CTCTTTTGTC TTGGGAGCTT 1320
TGAGAGAACA ATTTTAGTCA GACAAGAGTC AACTGACACC 1360
|
