| Tag | Content |
|---|
EnhancerAtlas ID | HS061-14469 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr2:134990850-134991990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr2:134991327-134991338 | ACAGATAAGGA | - | 6.14 | | RORA(var.2) | MA0072.1 | chr2:134991139-134991153 | TAAAACTAGGTCAG | + | 6.95 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_10191 | chr2:134988854-134992559 | CD19_Primary | | SE_10845 | chr2:134983475-134995336 | CD20 | | SE_18527 | chr2:134986976-134995300 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19349 | chr2:134988445-134994894 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_32531 | chr2:134988813-134993293 | GM12878 | | SE_58311 | chr2:134974519-135073637 | Ly1 | | SE_59645 | chr2:134963734-135083692 | Ly4 | | SE_62223 | chr2:134937777-135083863 | Tonsil |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I134231 | chr2 | 134988673 | 134994007 |
|
Enhancer Sequence | GGGGTATTAC TATGGGTCAT AATGAATTCA GTGGAATGGA TTTCAGACTT TTAGGTGCTG 60
ACCCAGAAAA TTCTTTGAAG TAGCAATCTT TACCAATGCT AGGAATTGGG CTAGTCTGCT 120
TTGCTTCCTC ATCAAAACTG ATGGACAAGA TAGAAAATGC CTTTTTATCA GTTACAGTAA 180
CATTTTGCTG ACACTTGGTG CATTTTTTTT ATGTGTTTCA CACAGATATG CTTACATCCT 240
TTGAGAAAAG GAACTGAAGG GAAGAAAGAA AACCACAACT GCTTTAGAAT AAAACTAGGT 300
CAGCAAAGGC AGATCTTAAT GTATTTAGAT CAGGCAGAAG GCTAGGTCCT TCCACCTTAC 360
TCACAGAGGC CTCTGGGGCT CATTGTAGGA GTCATGAGAC TTCTCCAGTA ACTCTCATCA 420
AGGATCGGTC ACTAGACTAG GCCCTTTGCA AATTTAAACC CTGCAGGTAG ACATTTTACA 480
GATAAGGAAA CTGGATCTTC ATTTCTGTAA CTTCAAGAGG GCACAGGGCT GGCTTATGTC 540
AGTGCAGAGA TTTTAATCTG AATCTAATTC CCAAGCCTCT CTGCCACACC AGATTGCCTC 600
TCTATTCATG CACAACACTC TAGGTTTGAC TCTGGCTCTC TTGAATAATT CCGAAGCAGA 660
CTTCTAAGAG AGGATTGCAA AGGCCAACTT CTTTCACAGC TGAGAAGCTG CCTTCTGAGG 720
TGTATCTCTG AGTGGAGAAA TCAGAACGCT AGATGCTATG TCCTTTCATG ATGGGTAATA 780
ATCTCATTAG AGCAGGGAGA CTTTGTGGTC TAAAGAGAGA AGGAAACAGT CAGTTGAAAG 840
TTGCTCATGT GTTTCATTTT TCTGTGTTTC TCATACTTTG TTATTGATGT GATGAAGTAG 900
TTGGGGGCTG AGAAGGAAGC CGGGGATTGG GGGCAGGGGT TGGTGGGAGT CAAGACTTAC 960
AGGTTCTTCC AAGAGACTCC TAGAGCAGTG ATGCCTATAG TTTGCAAGGG CACCACCAGC 1020
AGCCATCTTT ATTAACCAAG GGGGCTACAA GGACTTTTCC CAACAGATAT TAAGTAGTTA 1080
GTTCACAGAA AGATTTGAAT CTCTTCCTTC AAGAAGTTTG AGTCTCAACA GGGAGCAGAT 1140
|
