| Tag | Content |
|---|
EnhancerAtlas ID | HS098-11093 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:100609480-100611770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr11:100611341-100611357 | AGTTCTTGGAAAGCAG | - | 6 | | MAFK | MA0496.2 | chr11:100611056-100611075 | ATTTGCTGAGTAAACACTT | - | 6.03 | | MAFK | MA0496.2 | chr11:100611056-100611075 | ATTTGCTGAGTAAACACTT | + | 6.22 | | MNX1 | MA0707.1 | chr11:100609989-100609999 | GGTAATTAAA | + | 6.02 | | TEAD1 | MA0090.2 | chr11:100611322-100611332 | ATGGAATGTG | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I100738 | chr11 | 100609169 | 100613145 |
|
Enhancer Sequence | AAATAAAGTG AACATGTAGA AATCTGTTTA TTATTACGTT TCAAGTTTGA ATATTTTGTT 60
TTCTTTTTAA GAAGAAGCAG GGCAAAACAA ACTGTGCCCG TTGCATTCCT TGCCAAGGTC 120
AATGCTCCAT ATTTTGTCTG ACTGTTTAAT TTAATAGCAT TCAAGCACAG AAGCAATCAG 180
GAGGCCACTC CTATTGGTAA ATCCATGCTT ATAAAGAAAG CATGTATTTC AGAACTTAGG 240
AAAAAAGCTG TTTGTTAAGC CCAGACCTAG TTTGAGATCT TTTTGAAAAG TGCTTATAAT 300
TTTCCAGAAT TCTAGGATTA ACTCAAGGAA ATGCACAACA GAAATATGTA GATTTGACAG 360
TGGCTTTTTT CTTCTGTTCA AGTTATCTTA GAGTCTTTTT TTTTGTTTTT GTTTTTGTTT 420
TAAATGAAGC AGTTTTGAGA TTCATTAACT GGTTATCTTT TGTCTGAGTT TTACCAAAGT 480
GATCAAAAAA TAAGGAACTA TTGACTTTTG GTAATTAAAA TACTCTTGGA TTTTTTTTTT 540
TTAGTTAAAG TTCAGGACCA TTCACTTGGT TCTTAAACAA TCTTGTTTTA ACCTGAAGAA 600
CTCTTGATTT GAAACTTTGA AATCCTGAGA AACATTTTTT CTATGACTCT CAAAAATAAC 660
TTCAGATTGC AATTTGTTCT AAAGAGGATA AAGTAGATAT ACCATGCTTG TTTTCTTTTC 720
CTTAATTGAG TTTCATTTAT GTGATTAACT TAGATAAAAA TACTCTAATT TGATTTACTG 780
AAGCAGTCAG GATGAAATAT TTTGCATAGT GAAGTGTGCT AAATCTTTAA AACTATTTCT 840
AGAGTTTTTA AAGAAAGAAT TTTAAAATGT AATGTACGAA GGTATAATTC TGTGTATCTA 900
TACTTTGTTT CTCCCTCCCC TCTGCATCTA ATAAGCCCCT CTTTTCTTGT TCCTTTTGTA 960
AACATGAGTT GCTTATGGCT TGTGTACTGA AAATGCTGCC AGGAAGTAGG GTGAGCATAA 1020
CTTCTTTTCC CATGACCCTC AGTCTAATGT TGTTCCAAGG GTTCCTTACT TAGAAATGCC 1080
TTGATAACCG CATTCATTCC TGACATACCC CACCCCCAAC ACACACAACT GCTGAGTGCC 1140
ATCTGACCCA CAGTCCAGCT GCAGCTTTTA AAAATACTAG TGGCAAAGGC TTTTACCTAG 1200
AACGGTGACT ATCTGTGAAA AAATTTTGTG TGTGATTTGT TTTTTGCGTG TTGAAATATT 1260
ATTTTTTAAA GAAAGTTACT TGGTGTCAGC CTGCAAGTTA AAGGGTTATT AGTACAATTT 1320
TTTTTTTTTT TTTTAATTTT CAACTCACTA AAGCTTGCCT GTGTATGTTC ATCCTTTTTG 1380
TATGATTTCT GGAAGTTTTC CTGTTGACAG TGAAGTCTAA AATGCTAAGA CCTTTAGATT 1440
CTCTTGTTTC ATGACTTTTA TTATGAACAT AAAACTTTTA AAAAAGACCT GGTCATGCTA 1500
TGGCCTCTCC CTTCTCCCAA ATTTTATATG ATACCCTCAG TTTTTTTTCC TTTGGTGCAC 1560
AAGGGAAGAA AAACGTATTT GCTGAGTAAA CACTTGGGCA CTGAATTTAT TTCTCCCATC 1620
TTCTAAAAAC TGTGAAGTGA GCACTAGCGT TCTTTTATAT GTAGAAAATT GAGAGTGCAA 1680
AACAGGTTAA CTAATTTGCT CCAGGAACAA AAGCTAGTCA GTCATGGAAC TAAGATTTGA 1740
ACCTGTCTGT CTGATACTAA AGTGCTATTC TTTGCCATTT GAAGGCAGTA TCATTCATGC 1800
CATGAACATT AGCCAGAAGC TTTATGGTAT AGGGGGAGGA GAATGGAATG TGTAGAGGAA 1860
AAGTTCTTGG AAAGCAGAGT TTGATGTAGA ATGGTTCCTG AAAGTGAAGG GGATGGTGCC 1920
AGCAGTTGCA AGATAAAGCG ATGGGGTAGG TACATTGCTC CTGGCAGCTG CTCCTTCTGC 1980
CTCTCCTGTT GTTGAGTGTC AGATTTTGCT GCTCCAGGGA AGATTCAACC ACTGTTAAAG 2040
TTTGGCACAG GGTTGATGAA GCTTTGGAAC GTTACTTACT GGATTATTTA AAAAAAATAT 2100
GTCTATCAAG AGAAGAATAA AGAGGGTATC TGTGGTTATA CTTTAATTAG TTATTCCTGG 2160
AGAGGGGACA TGTGGCCTTA TTCTAGTCCC ATGGGCTTGA GGGGGAAAGC AGACAGATTT 2220
ATTTGACTGA CTGTAAGGCT CCTTTGCAGA TTACATAAAG AGAGAAAATA AGAAATTTTA 2280
TTTATTTATT 2290
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