| Tag | Content |
|---|
EnhancerAtlas ID | HS092-10928 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:130500180-130502560 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:130501520-130501541 | ACTTTCTTTCTTTTTTTTTTT | + | 6.09 | | YY1 | MA0095.2 | chr11:130502191-130502203 | GCTGCCATTTTG | - | 6.18 | | Zfx | MA0146.2 | chr11:130501776-130501790 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I130630 | chr11 | 130500621 | 130501562 |
|
Enhancer Sequence | TTATTTATTT TCTTTTTTTT TGGAGACAGG CTGTATAAGA CTCTGTTGCT CAGGCTAGAG 60
TGCAATGGCA TGATCATAGC TCACTACAGC CTCCAACTCC TGGGCTCAAG CAATCCTCCC 120
ACCTCAGCAT CCCAAGTAGC TGATACTACA GGTACATGCC ACCATGCCTG GTTAATTTTT 180
ATTTTTTATA GAGACAGGGT CTCATTATGC TGTCCAGGCT GGTCTTGAAC TCTGGGCCTC 240
AAGTAATCCT CCTGTCTCGA CCTCTCAAAG CGCTGGGAGT AGAGAGAGGT GTGAGTCACA 300
GTGTCCAGCC TAGTTAACGC ATTTTTGGTA CTTTCCATAT GTCAAGTGTT ATACTGATAT 360
TATATAATTT AATTTTCACA ACAGTCTTAT AGGTAGTATA GTATTGTTTT CCTTTTATAG 420
GCGATGAGAC GGAGGCACAG AGAAGTTAAG TAACTTGCTC AAGGACAACA GTTAGCAGAT 480
GACAGAGACG GAGTTCAAAC CCAGGCTGTG TTCCCGGCAC TCCTTTAGCT ACTATACTTT 540
ACTGCCTGTT GTTTTATGAT TCAAAGACGT GAATCCATGA ATTGAGCGTG TTGTGTGTGT 600
GTCTCCCAAA ACTACAGAGT AAGAAGTAGG GTAAGAGTAG GGAGTGGGCT GGGTGCGGTG 660
GCTCATGCCT GTAATCCTAG CACTTTGGGA GGTGAGGGTG GGCTGATGGC TTGAGCCCAG 720
GAGTTTGAGA CCAGCCTGAG TAACGTGGTG AAACCCTGTC TCTACAAAAA TTACAAAAAT 780
TACCTGGGCA TGGTTGCACA TGCCTGTAGT CCCAGCTCCT CAGGAGGCTG AGATGTTGAA 840
CCTGGGAGGT TGAGGCTGAA GCAGCATTCT AGCCTGGGCG ACAGAGTGAG ACTCTGTCAA 900
AAAAAAAAAA AAAAGGAGTG GTTTATTGTA AATGGAGGTA GGACTAATTC TTGAACCATA 960
TTGTGGTTTT GCAGGAGGTG AGTCAGATGG CTTTTGGTGA GTCAGATGGC TTAGTTAAGT 1020
TGACCCAGCT ATTGGGATGG GTTGTGCAAA GCCCAGGCAC AGGGTTCAGA CTCCATCTTC 1080
TGTGTTCTTC TTAATTGACA AACTGCAATG GCTGTCTTCA GAGTCTTGGT TTTCTATGGT 1140
GGTCAACTCC TGAGTTCTTA TGATGTCGCT GGGCACAGAA AAAATAAACG GAGAAGGTAA 1200
GGTAAGAAGG GAGTCCTTAT AAAGGTGGAG CTGAAGGGTG TTTTAGGGGG ACCACTCCAT 1260
CTCTCTGTCT GTCATTCAAA GGCACAACTA TGCCCAATGA CTTGGAGTAG CAGGTCTGAG 1320
GGGCGTTTAG GTTGATCCCT ACTTTCTTTC TTTTTTTTTT TTTTTTTTTG AGATGGAGTC 1380
TCACTCTGTC ACCCAGGCTG GAGTGTAATG GTGTGATCTC AGCTCACTGC AACCTCTGCC 1440
TCCTTTGCTC GAGGGATTCT CCTGCCTCAG CCTCCCAAGT AGCTGGGATT ACAGGTGCCC 1500
GTCATCATGC CTGGCTCATT TTTTTGTATT TTTTAGTAGA GACAGGATTT CACTATGTTG 1560
GCCAGGGTGA TCTCGAACTC CTGACCTCAG GGTCCGCCCG CCTCGGCCTC CCAAAGTGCT 1620
GGGATTACAG GCGTGAGCCA CCGTGCCTGG CTGATCCCTA CTTTCCATGG TTAGTTTCCC 1680
AGGCCTTGGT TTATGAGCAA TAAATTCTCC CATGAGGTTT GTCTTTTCGT TTTATTGGAG 1740
GACGTTTTCT CATAAAGTCC CTTTCCAGGC CATCAGAACT CCCCAAACTC TTGGGAACTG 1800
CATTCCATCT GCATGCCTTG TGATTTCCTT CCCCCCAACC CCCACCAGTG TATCCTCTTC 1860
TCTCTCCTAT TAGTAGTCAG GATGGGCTTT GCACGACCCA TCTCAATAGC GGGGTGAACT 1920
CTAAATAAGC CATCTGACTC CGTGTCAGTC TTTCTCTCTC TCTGTCCACC CTACACCAAC 1980
TTATGATCCC AAGAAACTTT GTTTTCCTAG GGCTGCCATT TTGAAAATGT TGCTTCCTAC 2040
TCTAGGAACT GCTTTATGAG TAAGAGACAC CTCTCCATTA GTCCATGAGG TTAATAATAT 2100
AAATCTATAG AGAACTTAGG TACCATCCAG TTAAACCAGG CTCTTAACGT AAGGATTGTC 2160
TTTACAGTGT TTATGTCAAG CAGTCATCTA GTGGCTGGTT AAACATCTCC AGTGACATGG 2220
AACAGTCAGT TCAATTTTTA GACAATTCTG CTAGAACCCT TTTTGTTATA GCAGAAATGA 2280
GATATCCATA GTGCCCACTA ATGGGACAAT GGGATGTGGA TGTGTCTGTA AGAATGTGAA 2340
GGTCTTTTTA TGGGTTTTCT CCATTATTCA CCCCAATAGT 2380
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