| Tag | Content |
|---|
EnhancerAtlas ID | HS055-02701 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr14:105896150-105898900 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr14:105898314-105898331 | TGAACTTCATTTGACCT | - | 6.37 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I105430 | chr14 | 105896961 | 105897338 |
|
Enhancer Sequence | TGGTGCGATC TTGGCTCACT GCCACCTCCA GCTCTCGGGT TCAAGTGATT CTCCCACCTC 60
AGCCTCCCGA GTAGCTGGGA TTACAGGCAC ACACCACCAT GCCTGGCTAA TTTTTTTATT 120
TTTAGTAGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCAAACTCC TGACCTCAAG 180
TGATCCACCT GCTTTGGCCT CCCAAAGTGC TGGGAATACA GGTGTGAGCC ACTGCGCCCG 240
ACCCACTTTT AGTTTCTTTC AGGAACTTTT CCTCTGCATT CACAACTGGG CTACCTGCTT 300
GGCGCTGAAG ACCAGGCTTT CCGTTAGGGT ATCTTGGCTT TCGACAGGCC TTCCTAACTA 360
AGCTTAGTCA TTTATTTCCA GCTTTTGTTT TAAAGTGAGA GATGTGTGAC CCTCAACTCT 420
TCCCTTCACT GGACTACTTA GAGGCCATGG CAGGGTTGCT AGTTGGCCCA ATTTCAGTAT 480
TGTTGTGTCT CAGGGAATAG AGAGGCCCCA GGAGAGGGAG AGAAATGGAG GAATGGCCAG 540
TTCCTGGGGC AGTCGGAACA CACACATTTA TCAATTAAGT TCTTAGTTGG GGTATGGCTC 600
ATGATGCCCA AAACAATTAC AATAGTAGCA TCGAGGAGCA ATGACCACAG ATCGCCATCA 660
CAGATAGAAT CATGGTTAAA AAGTTGGAAA TGTTGAGAGA ATTACCAAAA CGTGACAGCA 720
ACACGTAGTG AGCACCTGCT GTTGGAAAAA TGGCACCGAT GGACTTGACT TGATGCACGT 780
TGCCACAAAC CTTCAATTTG TAAGAAACAC AATACCTGCA AAGCATCATC AAGCTAAGCA 840
TGATGCCCGT GTAGATGTTT GGGAAATAAT TGGCATCTAA ACCAATCTTG GGTCCTCTCG 900
TACAGGGATT GGCAAACTGG CCCGCTGCCT GTTTTTGATG ACTCACGAGC TAAGAATGGG 960
TTTTACATTT TTTAATTGTT GAGAAAAAAA TCAAAGGCAG AAAACTTCAT GACACATGAA 1020
GATTATATGA AATTCACATT TCAGTGCTCA GAAATAAAGT GTTATGGGAA CACGGCCGCA 1080
CTAATGGGAG GGATTCCAGT TATTATGTGG CTGCTTTGAG CTACCGTGGT GGGGTTGAAT 1140
ATTTGTGATA GGGACAGGAA AAACTTAACT TTTTCCCAGT CTCACACGTT CAACACAGAA 1200
CACTTCACCT CTGGTCCCTG GAATGTGTGT GGGGTTTCTC CCTACCAGCA GCCAGTCGGT 1260
TATCCAGTGA TTTAACCCAA TTTTGACACT GCTTACCTGG AGAGAATATT AGGTTCTGCA 1320
GCTGAAGGGC TGAGTCCCAC AAGACTGTCC TCACTTCTCC TGCCTCAGCC TCCCGAGTAG 1380
CTGGGATTAC AGGCGCCCAC CACCACGCAC AGTTAATTTT TGTATTTTTA GTAGAGACCA 1440
GGTTTCACCA TATTGGCCAG GCTGGTCTCA AACTCCTGAC CTCAGGTGAT CCACCCACCT 1500
TGGCCTCCCA AACTGCTGGG ATTTACAGGC ATGAGCCACT GTGCCCAGCC TACAAGCTGG 1560
TTATTAACAA GACCAATAAA CTGAAATCTA TAGCCAGACT GACAAAGAAA TAGAAGCCAC 1620
AAGTAACCAA CATCAGGAAC AACAGATGGG ACATCACTAC AGATCCTACT GACACGAGAA 1680
ATGTGTGGCA CAGAAAAGGG CTTGGTTGGA CAAATTTACA AGGGTTGTTA AACATACAAA 1740
GTGCCAAAAG CCTATAGTTA TTCATTCTAT TACTTGTTGG CAGGTAAATA TTTTGTGGAA 1800
AGTATTTGTT TATTTTTATT TTTACTTTTT GAGGTGGAGT CTCGCCCTGT TGCCCAGGCA 1860
GCAGTGCAGT GGCGCAGTCT CGGCTCACTA CAACCTCTGC CTCCCGGGCC CGAGTGATTC 1920
TCCTGCTTCA GCCTCCCAAG TAGCTGGGAC TAAAGGCATG CACCACCACA CCTGGCTATT 1980
TTTTGTATCT TTAGTAGAGA TGGGGTTTCA CCATGTTGGG CAGGCTGGTC TCAAACTCCT 2040
GACCTCAGGT GATCCGCCCA CCTCAGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGGCA 2100
CTACACCCGG CCTGTGGAAA GTATTTGAGT CTGTCATGCC TTATTGAACC AGTAGTGTCA 2160
ACAGTGAACT TCATTTGACC TTGTGGACTT GATGTCATCA GTTCTGTGAA TTAAAAAAAA 2220
ACCTTTTTTA AAGAGATAGA GTCTTGCTTT ATTGCCCAGG CTAGAGAGCA GTGGCACAGT 2280
CCTGGCCCAC TGCAGCCTCA ATTTCCTGGG CTCAGGTGTG AGCCCCTGTG CCTGGCCTAA 2340
AGCTGAACAT CTTGACTTGC TGTCCTGTGC AGCAGCTTGA TGAGTTGGCA GTGGTGAAGT 2400
TCTATTGCTT TTTTATTTTT ATTTTTTATT TATTTATTTA TTTTTGAGAC GGAGTCTTGC 2460
TCTGTCACCC AGGCTGGAGT GCAGTGGCGT GATCTCGGCT CACCGCAACC TCTGCCTCCT 2520
GGGTTCAAGC AATTATCCTG CCTCAGCCTC CCAAGTAGCT GGGATTACAG GCACATGCCA 2580
CCATGCCCGG CTAATTTTTG TATTTTTAGT GGAGATGAGG TTTCACCATG TTGGCCAGGC 2640
TGGTCTCAAA CTCCTGACCT CATGATCCAC CTGCCTCGGC CTCCCAAAGT GCTGGGATTA 2700
CAGGCGTGAG CCACCGTGTC TGGCCTGCTT TTTGAAAAAG CGCCGAAATT 2750
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