| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12456 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:45226770-45227880 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr19:45226881-45226902 | GAAGGAGGAGTAGGAGAGATG | + | 6.2 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_09606 | chr19:45225026-45227473 | CD14 | | SE_23197 | chr19:45226609-45227960 | Colon_Crypt_1 | | SE_23877 | chr19:45226698-45227829 | Colon_Crypt_2 | | SE_26699 | chr19:45226534-45229277 | Esophagus | | SE_31568 | chr19:45227174-45229356 | Gastric | | SE_34750 | chr19:45226424-45229782 | HeLa | | SE_47531 | chr19:45227242-45227666 | Pancreas | | SE_53360 | chr19:45226521-45227795 | Spleen | | SE_56197 | chr19:45227061-45227913 | u87 | | SE_62704 | chr19:45221152-45271677 | Tonsil | | SE_65330 | chr19:45226619-45230111 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I044721 | chr19 | 45225041 | 45229949 |
|
Enhancer Sequence | GCATTGTCAG TGTCAGGCCC CAGGGGAACA CAGCAGTGAC CACGACAGCC CCACCAGACC 60
ATGACCCTGA CCAGGGGGCT CACGAGGGCG GAGACATCTA CTCCAAGACC TGAAGGAGGA 120
GTAGGAGAGA TGCTGGGGAA GAGGCAGGGA AGGGTGTTCC TGGCAGAGGG AACAGCCTGT 180
GCGAAGGCCT GAAGGTAAGT TTTGCATATG ACACCTTTGA GAAACTACTT ATTGTTCAAC 240
TGAAGCATAG GGTTGTTCAG AAGAAGCCAG CCTTGTGGCC GGGTGTGGAC TTCCTCCCAG 300
GGCACCAGGG AGCCACTGCA GAGTTGTGAG CAAGGGACAG ACAGAGGTAG GCTTGTACTT 360
CCAAGAGACT CCCCCAGCTG CCACATGCAG GGTGAATGGA ATGATGCACA GAATCCAGTT 420
TCAGGGGTAG TTTGGTACTT GGACCCAGGT CCCAGGGAGA GAGTCCAAGG AGCCCTTCTC 480
TGGTCTTCCA AGGAGCTGCT CTCCCCAAGC TCCGGATGGA AGGCGTGCCC ATGGCAACCG 540
CTAGGTGGTG CCCGTACACC ACCAGCCAGG TCTTTTTTTG CCAAAAGTAG ATCAGGCCCA 600
GAGCTGGGCA GAACTGCCCC TGGGTCAGGA GAGCAAATCG TCTCTGTCTT TTGGTCCTGG 660
CTCCCTGGCC AGGCATCCTG GGGCCATTTG ACTCCCAGGC TCAGGAAGGA GCTGGCTGAG 720
CTGCAGTGAG TATGTTCTTC GTCTCTTTCC TCACCTTGGA ATCTCAGACG GGAGCACCCT 780
GGCTCCCACT TCAGACAGGA AGATTCTTAC CTCCCTCATC AGACTAGCAG GCTCTTTGTC 840
TCCCCACCAG TTTGAGGGGC TCCCCATTTC TATCATTCAT TTGGAAGCTC ATCAGCTCTC 900
CCAGAAGGCA TGGGAGCCCT TCAACACCCC CATCAGACTA GGACTACCCA TCTCCCCCAT 960
CAAATTAGAA CTGCATTGTC TCACACATCA AAGTATCACT CCTGGCCAGG TGCAGTGGCT 1020
CCCGCCTGTA ATCCAAGCAC TTTGGGAGGC CGAGGCAGGA GGATCACCTG AGGTCAGAAA 1080
TTCAAGACAA ACCTGGCCAA CACGGTGAAA 1110
|
