| Tag | Content |
|---|
EnhancerAtlas ID | HS010-00993 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr12:782970-783950 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr12:783874-783888 | GTGAGTCATTTCCT | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_11737 | chr12:781163-784829 | CD20 | | SE_62689 | chr12:719155-796233 | Tonsil |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I000671 | chr12 | 781086 | 785256 |
|
Enhancer Sequence | GCAACAAGAG CAAAACTCCA TCTCAAGAAA AAAAAAACAT GTATTAGCCT CTGAAGATTT 60
ACTGTGCTGC TGAGAGGAAC TTAAAGTTTG GTTCTTGGGG AAAGAGCTGT TAGGTAAGCT 120
GGGATGCAAT AGACATAGGT TCACAGAATG AACCCTTATG GTGGGCTGTG GGACAAAAAA 180
GTTTCCAATT TGGACCCCTC ACCAAGAGAA ACAGAAGGGG AAGAGAAAGT ACAGGAGGGA 240
AAAATCAAAG CGTGGGGGCG AGCTGCTGCT TTTAGCCATG GTGAAGGTGA AATCAGGAAA 300
CTTCAGTGGG GTTTGTCAAA GAAGACCTTC AATACATACT ATGAACTATG GAATATGCAA 360
AACGAGAACT ATTTTGTGCA TTTCTACCCC CTTCTCCTTC ATACTGTTGA CCTTCAGGTG 420
CCTACACAGG GTAGCTGGGG GAAATTAAAA GGAGCAGAGC TTCCAGCATT TTTTCTTTTG 480
TGAACAACCC TGGTAAAAAG ATTTTGTGCC AACGGTTCTT GGTTTCTCCT CTGACAACCA 540
GTTCCTTCCC CTGCTATTCT TACAGCATTC AGAGTCTGCA CAACAGCACT GACATCCCTG 600
CTTCATGTGC AACTGTGAGT ACCCATCTGT AAGCCTTTGA GAACAGGGAC TGTGGCTTCT 660
ACTTCTGAAA CTCCCACAGC AGTGAGCCCC TGCAGATAAG CACATACTAA CTGATACTGG 720
GCTTCTGAGG GGGGGCCCCC TTCTGCATAG TGTAGTGCTA GGTCCCCAGA TCAAGTCAGA 780
TGCCAACGAG ATTCTTGTTA GAAAAGCTGT GGGTAACACA GACCCAAGAG AGTGGGGTGC 840
AAAAATGGAA ATGCAGTTTC CTGAACATTG TCATAATGTG ACATCGATTG CTGTGTGATC 900
TTACGTGAGT CATTTCCTTC CCATCTGTTA CCTTGGTTTC ACTCATCTGC AGAATGAGAA 960
CAGTTTTGTA AAGGCACATG 980
|
