Tag | Content |
---|
EnhancerAtlas ID | HS091-08587 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:101955290-101957480 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr11:101956729-101956743 | TTTGTTTACCTTTG | - | 7.22 | POU6F1 | MA0628.1 | chr11:101956366-101956376 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr11:101956366-101956376 | ATTAATTAAT | - | 6.02 | Pou2f3 | MA0627.1 | chr11:101955795-101955811 | GATTATGCAAATTATC | + | 6.22 | Sox6 | MA0515.1 | chr11:101955758-101955768 | CCATTGTTTT | + | 6.02 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I102085 | chr11 | 101956701 | 101956850 |
|
Enhancer Sequence | GAAATGTCTG TTTGCTACCA GCTTTGCTGC TTACCTCACA GTTCCCTATG ACCTGGAGAC 60 CCTTTCGATC AATCAAGTGG CCAATCAGTA ATTCTTTTTG AATACCAATT CTGTGCAAGG 120 CACTGGGCAG TTTACTTTGG GGAAACATAC ACTCCCTATA AACCTATTTA GGAAGGTAAT 180 CTTTAAGAGT GTGACTACCA ATAGTGATTG TTGCATGAAT TCAGAGATAG AAGAGATCAC 240 TCTGAACTAA GATAGGCTTA GTCTGGCTTC TATGGAAAGA CTGGTGGGAT ATCAGTAATG 300 GAAGAGAACA GCAGTTGAAG GGAGCACATG ATGTGGCGAG GTACTCTGGG CTTGGCCCTT 360 GGATGAAAGT CCAGAGGCGA AAGATGGGAA AGTGATACTG AGGAATTGCC ACTATTTTTT 420 CTCCGCTCTA AAGGTGGAGG TAGATAGGAC CTTTGAGGAA AGATTGCTCC ATTGTTTTGG 480 AAAAATCATT TGATGACTCA TTTGTGATTA TGCAAATTAT CTGTATTATA AGGCATAATA 540 GAGTAGTGAT AAAGAGTTTG GGCTGGGCTG TCAGGTTGCC TGGATTTTTT AATTTGCCAT 600 TACTTGCTGT GTGACCTTGA GCTGGTTACT TAACTCTCTG CGCCTTAATT GTCTTTTCTA 660 TAAAATGGAA AAAAATAATA GGACTACCTC GCAGGGCACG GTGGCTAACG CCTGTAATCC 720 CAGCACTTTG GGAGGCCAAG GCAGGCGGAT CACGAGGCCA GGAGATCGAG ACCATCCTGG 780 CTAACACAGT GAAACCCCAT CTCTACAACA AAATAACAAA AAAAAAAAAA AAAAAAAAAA 840 AAAAAGAAAA ATGAGCTGGG CGTACTGGTG GGAGCCTGTA GTCCCAGCTA CTCAGGAGGC 900 TGAGGCAGGA GAATGGCATG AACCCGGCAG GCGGAGGTTG CAGTGAGCTG AATCGCGCCA 960 CTGCACTCCG GCCTAGGCGA GAGAGCGAGA CTCTATCTCA AAAAATAAAA TAAAAATAAA 1020 TAATAATAAT AATAATAATA GGACTACCTC ATAAGTTCCC TTTTTTGGAA AATTGTATTA 1080 ATTAATACAT ATGTTGGTCT TTGAATGATG CCAGGCACAT AGTTTAAGTG CTCATGAATT 1140 TTGGCTGCAT TCTCTACTGA GGAAATATGA AGAAAAAAAA AGAGAAACAG TTAACTGTCT 1200 GCATAATAAT GTAAAAAGCT GTCTTCTTGG GGCCAGAATT GCTTTTGTAT AGATTATTAT 1260 TAATTGACTG AAGAGATGGG AAAATTGGTT TTTCCTCTTT GGAGGCCCCA GAGAACGTAG 1320 AGGTCCTGAG CACGGACTCC AGGGATTTCT TTGGCAGCAT TTGTACACTT GGAACTATTT 1380 GCGCAGCTAT TTGTTATAAT TTGTTTAATA TCTTTCATGA AAACAAGTAC TGTGTCCATT 1440 TTGTTTACCT TTGTGTCCAC AATGCCTAGA ACTTGAAAGA CAATACATGC CTATTCTCTG 1500 ACTAAGTACT GTTGGTAGAG AGAAACTGGC CTTTGAAGTG CAACTGTGGA GACTGTGGAA 1560 AGCGAGGGAG GAGGAAAGGT TGGTGCTGAG AGTTATAGAT CATCAGCATG GAAGCCTCCT 1620 CTGCAGGGGC TGAGCTGGTG GACTCTAGCA GCCTTCATAC CTACGTGCCC ACCTTAAATT 1680 TACTGTACAG TCATCCCTCT AGTTATACTT CAACCTTTTG TTAAATTTTG CAAACTATTA 1740 TAGTCTGGAT TCATACTGTA GTCTGGATTT AGCTGCCCAG CATGGGATTA GATATGCAGC 1800 CCAGGAACAT GCCTGTGGCA AAAATTGTCC CTAGAGAGCA GCAGCCGCAG CCTGTAGAAG 1860 CCGGCTTTGT AAAAGCAAAC TGTGATCAAG TGAGAGAAGA GGGGTTGTCT GGAGTGAGAC 1920 AACTGGCCAT GGTGACAAGT GACCACAGAA TGGCTTTCTG AGACTTTCTG AGAGCATTCT 1980 TCAAAAATTC CAAAAGTATC TAGAACTAGA AATACCATTT GACCCAGCCA TCCCATTACT 2040 GGGTATATAC CCAAAGGACT ATAAATCATG CTGCTATAAA GACACATGCA CACGTATGTT 2100 TATTGCGGCA TTATTCACAA TAGCAAAGAC TTGGAACCAA CCCAAATGTC CAACAATGAT 2160 AGACTGGATT AAGAAAATGT GGCACATATA 2190
|