| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08686 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr3:4545590-4546980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr3:4546135-4546153 | TGAAAACGAAAGCATAAT | + | 6.26 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_10644 | chr3:4542662-4550173 | CD19_Primary | | SE_11257 | chr3:4533655-4563092 | CD20 | | SE_13171 | chr3:4545499-4547083 | CD34_Primary_RO01480 | | SE_13547 | chr3:4544776-4550219 | CD34_Primary_RO01536 | | SE_14254 | chr3:4544770-4547635 | CD34_Primary_RO01549 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I004502 | chr3 | 4544126 | 4550060 |
|
Enhancer Sequence | TAAGCACCCT CCCCCTCTCG CCCCCTCCCA AAACCAAAAA ACACTGGCCT TGGTATCTGG 60
AGCCCTGTGG TCTATCTTTG GGCACTCATC AGCTGTGTGA CCTCCAAGAA ATCACTAGGC 120
CTCAGGTTTG TTTTTTCTAC CCGTAAATTA AAGAGTTTTA GCTAAATGCC CTCCACTCAC 180
CAAATCTGCA GCTCTTTGCC TTGGAAATAT TGAGCTTTTG GTTGGCTTCT CTTACTTTGG 240
CCTTGAAGAA TAGAAGCCAT GAGACCAAAT GTCAGTGCGG GCATCTTTTT TTGAGAAATA 300
ACTTTGTAGA TATTGTACCT GGTTGGGGAA AAGGTTATTT AGCAGACATG TCTGAAAAAG 360
CGAGTAGGTT TATTTTTGTG TGTGTATGTG TGTTGCGGCG GGGGGAATGG AGAATGAGCA 420
ACGTTGTATT ATACTAGAGA ATCACTCCTC TGAACTTCAG ATTTACAGCT GCTGTTTCTG 480
GGAGGCCATG AAGGGCCTTG CTTAAAGATG AAACTTCTGA GTTGGTGACT TCCTTTGGGA 540
CTGCCTGAAA ACGAAAGCAT AATACAATTT TCTATGCTCC CAGAGAAGTG CTTTTTGCAA 600
GAGAATAAAT TATCTGATGA TGGGGACATG CTGCATTTCT GAGGACGATC TGATTAGCAG 660
CTAATGGGAC AAGAAGGCAA GGAGGGGGAG CTGTGTGAAA ACGTGTGGGG AGGAGGGTGG 720
CATTATGTCC AAGTCAAAAA TGTGCTGTTC CTCCTCATTT CACAATAAAG ATGATATCGC 780
CAAGCATCTT TGCTCAAAGG AAGTCCAAAA TTAACCCTGA GTGCCCAGGA ACAGGAGCAG 840
AGACTGTTGT AAAGGGAGCC TTTTTCTCCC TCTTGAAAAA GTCAACCGTA AATGCGTTAG 900
GTTTTCTCTA CCTCGTATTT ACAGCCATAT TACCATATAT GTACCTGGGT GAGGGCATCG 960
CAGGGAGACT TGTGCTCACT CTGTAGGGAG TTTCCTTGGC CTCTTGCCAG GAGATTGATC 1020
AAATGCCAGC ACCTCTTCCT TTTTCTGGGC ATACTCCTTT TTTTTTTTTT CCTGTGAAAG 1080
ACCTCATGGT TTGCCAGGCT CGGCCCATCG TTAACCTGCC CTGCTGGGTG CTGCTTGACC 1140
TAAAAAGTGA AACGGTGCCT TTTTGTCTTC GTCCTTATCC TCGGTTCTGA GGGGCCAACT 1200
GCCTTATGGC CTCTTGGCTT GCCAGGTGCT TTGAGCAAAA GCCCTGTGTG TAAGCCCCTC 1260
TCTTTGCTGC CTAACTTTAA AGGAAGCTTT TTTCCCCTTG TTTTTGAGAA GGAGTCTCAT 1320
CTGTCGCCCA GGCTGGAGTG CAGTGGCATG ATCTCAGCCC ACTGCAACCT CCACCTCATA 1380
GGTTCATGCG 1390
|
