| Tag | Content |
|---|
EnhancerAtlas ID | HS098-11622 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:122188740-122190570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:122189033-122189044 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr11:122189033-122189044 | GGTGACTCATG | + | 6.02 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH11I122316 | chr11 | 122187661 | 122188867 | | GH11I122319 | chr11 | 122189909 | 122190108 | | GH11I122320 | chr11 | 122190309 | 122191308 |
|
Enhancer Sequence | AGATTTCAGT GAGCCAAGAT CGCACCACTT TAGTCCAGCC TGGGCGACAG AGTGAGATTC 60
TGTCTCAAAA AGCAAAGCAA AACAAAAAAC AAATTAGGTC CTTGACTCAT AGAACTTACA 120
TTCTAGTGGG AGAGTCAAAC ATGAATCAGG TAAGTGCACA GGTTAACATA TAATTGCAAA 180
TTGTGATATA AGTACTGCAA CTGAAAAGAA GAGGAATGAT TATGTCTATC TGTAGGGGAA 240
GAATTCCCCA AAGAAGGGGC ATTTAAGCTT ATATGAAGCA TGAAGCCAAG TGTGGTGACT 300
CATGCCTGTA ATTCCAGCAT GTTGGGGGGC CAAGGCAGGA GGATCATTTG AGGCCAGGAG 360
TTCAAGACCA GCCTGGCCAA CAAGCGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC 420
CAGGCGTGGT GGCAAGCACC TGTAGTCCCA GGTGCTTGGG AGGCTGAGGT ATGAGATTCG 480
CTTGAACCCA GGAAGTGGAG GTTGCAGTGA GCCCACATCT CACCATTGCA CTCCAGCCTG 540
GGCAACAGAG CAATACTCTG TCTCAAATAA ATAAATAAAC AAATATGAAG CATGAGATAT 600
AAGGAGCGCC ACCAGCTTTG AGTATAAAAT CTTCATGAAC ATTGGCTTGG AGAAAGCTGC 660
CACCAGGTTG AAGAAATTAC CAATACTGCC CACCGGAAGT TACACGGCCA CTGGTGAGCA 720
CCACGCTAGA CGACCAGAGA TCCCTGGGTA TCTGAGCTTG CCAGTTCTTC ATTAAAGGAG 780
GCAAAGGTGA GGCAAATACC AGTTTAGTCC TGCCCACCAC GAGGAAGGAA GGCAAAGTGT 840
GTAGTCATGA ATCCTTTTCT GTGGGCTTAT TCCTCCTTCA GCACCTAATA TGTATGTCTC 900
ATAAAAGGGG TGCTTATTGG AGAATGACTA GCACAAAGCT CTGTCAGTAT AAATCACAGA 960
AGCTTTGATC ATTGCTGAAG GTGGAGGATA TGGGTTATAA GGTGGGCAGG ATGGTCCCTA 1020
CAACCTGCAT AGGAGCAGTC TCCAGGGAGA GAAAGGAATG AAATCTCAAT TCCTGTATAA 1080
GCTACACAGA CATTAAGATG TTTCTCCCAA GCCCTCTATT TTCTACCAGT TTAAATCCAG 1140
CACATTCCTC AGAAGCCAAT TCAAGACTGG CCTCATTCCA TGAAACTTCC CTACATCCCA 1200
GAGCATGTCG TCTGCCCCCA CAGTATCATC CTTCCACTGC ACTGTGCTGT ATTGTTCTCA 1260
AGTCACTCAG TGAATTATTT TCTTGCCCAC TCAATAAGAT GATATACTCC TCAAGGACTA 1320
GGACTATTCC TTTAGTTCTT TTGTATTCCC CACAGTGCTG TGCTTAGTAT TGTGCCCACT 1380
CTAGGCACTT AACATATCAA TGCCTGTTGG GTAAATGAAT GGTTTAATTA ATCCATATAT 1440
CTGTAAGATT TCAGTAGGTG GGGAAAATAA AAAGAAGTGG CTCTGAGTAT AACAAAATTG 1500
AGCCATCCCT GGCTGGGGCT GGACAGTTAT CTTTAGGAGA GTGTTTAATA CTGTATATTG 1560
GTTCTTATTT AAACAGAGGG CTTAGGGTCC TATATCTGGA GATTTTCATC TGTCTAGGGT 1620
AATTGAAGGG CACCTCTGCC TGGCAATAAG CGATGGTCTA GGAAGACCTT TCAAAGCCCT 1680
TTCCATTTCT AATTCTGATT CTGTAGATTA GGATGTGTTA CCATCTCAGT CCAGAGAGTA 1740
CATGGTGTGA ATGTTAGCCA GTCCTTACAA CAGTCCCTGA ACCATCTCCT GCAAAGATCT 1800
CTAGAAACTC CAGACCCCTT TGTGAGCTCT 1830
|
