| Tag | Content |
|---|
EnhancerAtlas ID | HS182-15444 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:10314760-10316090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr3:10315649-10315662 | TAATTAATTATTA | + | 6.18 | | Lhx3 | MA0135.1 | chr3:10315645-10315658 | GAATTAATTAATT | + | 6.29 | | Lhx3 | MA0135.1 | chr3:10315646-10315659 | AATTAATTAATTA | - | 6.78 | | POU6F1 | MA0628.1 | chr3:10315647-10315657 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr3:10315647-10315657 | ATTAATTAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_19770 | chr3:10314718-10315309 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_62498 | chr3:10211834-10316085 | Tonsil |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I010273 | chr3 | 10314719 | 10315309 |
|
Enhancer Sequence | GCGACCTGCA CAACAAACTG AACTAGAAGC GATAGGCATA GGGGGATAAA CACAGTCTTG 60
AAGATGTCAT TTGGCTTGGT GAGATTTGAC TCAAGACTGG AAGATAATGA GTCTGAGGAG 120
TTGCTGGCTG GGAGAGGGCT AAGCTGCCTG TAAAGGGGAG GAAGACTAGA AAATATTTGT 180
CAACACCAGA GACTCCTAGG CTGGGTGGGG GATATGGACA CTGTTTTGAT GTAAATAAAA 240
AATTTGGCAC CCAAATGAGG TGAATGGTGG TGACTGGCAA CTGCACCTAG TTGGATGTCA 300
GTGCTGAGTT GCATTTACCT AAAAGAGCAG TTAGCAAGTT CTGGATGTGT CCTGCTGAAT 360
GTTTTATCTT GTGAAGGGAA GAAGAAGAAC CTATAGAGGG CTGGGCGAGG TGGCTCACGC 420
CTGTAATCCC AACACTTTGG GAGTCTGAGG CAGGAGATTG CTTGAGCCTA GGAGTTCAAG 480
ATGAGCCAAG GCAACATAGT GAGACCCCAT CTTTATTACA TTAAAAAAAA AAAAGAGCCT 540
GTGGAAGGTC TGTATCTGGG CAAGATGATA GGGTGACAGA CCCTGCTCAT TATAGGAGAG 600
TTTGGTTGAT GTACCTAAAA TTTTCTGGAA GGATTGGAAA ATAGAGAAAA GCAAAACAAT 660
TGGGGAAAGA ATGGGTAGTT ATAGTTATTC TGCTGGTTAG AGCAAATTAC TGTTAACGTT 720
TTCTTTGTTG ATCTGTGGTG TTTACAGATT AACTATGTAA CTCATAAGAG TTAGATCCTG 780
AATAGTTTGT GTGTAAGTTG CACATGTCAG CATCTGGGAG GGATGCCAGG GAGAGTAGAC 840
TGTCCTTCCC TACCCAGGCT GTATCTCTTT ACTTGTGTTA AAGAGGAATT AATTAATTAT 900
TAAAGTAATA AATATGCAAG AGATGCCTGG GGCAACTCCC AGGAGAGACT AACTCTGGAA 960
TCCCTGGAAA TAATGGATCA GTTAGGAAGC CAACCTTATG CAGGTAGAAG TGAGTAATTA 1020
TACTGGGTAA TAACTCATCT GTACTTCCTT CACTCCTGTT GTTTTTCAGC TGGGTTCCTG 1080
GTGAGGACAA ATGCTGCAAA TAGCTCCTGT CCAACCACAA GTTCCTGCAT TCTAATGAGT 1140
TCTTCTTCCT TCTTAACATT TTTGAAATCT GGATGTGTTT CATGAAACAT TATAAATGTA 1200
ATGTTATTGT TCCTTGGAAA ATTGCAAGGT ACAATACAAT TGCAAGGAAC AGTTGCACAG 1260
TGGCTTGTCT TCCATGCACC TGTCGTAGGT TGGATGTGTG TGCTTGTGTT AAAGAAAGAA 1320
ATTAGGAAAT 1330
|
