| Tag | Content |
|---|
EnhancerAtlas ID | HS047-10638 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr14:93029250-93033860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr14:93032146-93032161 | GGGTCTTTGTGACCT | - | 6.34 | | Foxd3 | MA0041.1 | chr14:93033630-93033642 | AAACCAACATTC | - | 6.04 | | Foxd3 | MA0041.1 | chr14:93029707-93029719 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr14:93029711-93029723 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr14:93029715-93029727 | AAACAAACAAAC | - | 6.32 | | MAFF | MA0495.3 | chr14:93031185-93031200 | CAGCTGACTCAGCAA | + | 6.4 | | MAFF | MA0495.3 | chr14:93031185-93031200 | CAGCTGACTCAGCAA | - | 6.57 | | MAFK | MA0496.2 | chr14:93031183-93031202 | AACAGCTGACTCAGCAAGG | + | 6.24 | | MAFK | MA0496.2 | chr14:93031183-93031202 | AACAGCTGACTCAGCAAGG | - | 6.56 | | MEF2A | MA0052.3 | chr14:93029539-93029551 | GCTAAAAATAGA | + | 6.92 | | MEF2B | MA0660.1 | chr14:93029539-93029551 | GCTAAAAATAGA | + | 6.44 | | MEF2C | MA0497.1 | chr14:93029537-93029552 | CTGCTAAAAATAGAA | + | 7.06 | | NKX2-3 | MA0672.1 | chr14:93032624-93032634 | TTCAAGTGGT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr14:93029488-93029503 | GAGGTCAGGAGTTCA | + | 6.22 | | SPI1 | MA0080.4 | chr14:93030889-93030903 | AGAAAGGGGAAGTG | + | 6.22 | | SPIB | MA0081.2 | chr14:93030891-93030903 | AAAGGGGAAGTG | + | 6.07 | | STAT1 | MA0137.3 | chr14:93031898-93031909 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr14:93031898-93031909 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr14:93031898-93031912 | TTTCTGGGAAAGGG | + | 6.56 | | YY1 | MA0095.2 | chr14:93032670-93032682 | CAAAATGGCAGC | + | 6.18 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01700 | chr14:93029785-93030566 | Aorta | | SE_01700 | chr14:93030583-93031883 | Aorta | | SE_20136 | chr14:93033230-93038028 | CD56 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I092562 | chr14 | 93029254 | 93033860 |
|
Enhancer Sequence | CTCTTTTAAG GTTGCTTTTG GTGATGAAGG AGGTGAAAGG TTGGGTCAAA AGTTGTAGTA 60
ACCTGAGTTG TGATATAGAC CAGCCATCTA GATGGTTCAA GGCACCCTCC CTAGGTGTGA 120
GCCCAAGGAG TACCGATTCT GTTGAGTATT AGTTTGGTAA AAACCTTCAG TGGGCCAGGT 180
GCAGTGACTC CTGCCTGGAA TCCCAGCACT TTGGGAGGCC GAGGTGGGTG GATCACCTGA 240
GGTCAGGAGT TCAAGACTAG CCTGGCCAAC ATGGTAAAAC CTCATATCTG CTAAAAATAG 300
AAAAAAATAG CCAGGAGTAG TGGCAGGCGC CTGTAATCCC AGCTACTTGG GAGGCTGAGG 360
CAGGAGAATC GCTTGAACCC GGGAGGCAGA AGTTGCAGTG AGAAAAGATC GCACCACTGC 420
ACTCCAGCCT GGGCAACAAG AGCAAAACTC TGTCTCAAAA CAAACAAACA AACAAACAAC 480
AAACTTCAGT GAAGCCCCTC TGTTGTGAGA CCAGGGAAAA AGGCACAATC ATCAATTATT 540
GCAGGATTAC TTTGGACTAA GCACCATCTC TCATTTTTCC AACAACCCTG CAAAACAGGG 600
GTGTGATCTC TATTCTATAA GGGAGGAAAC TCAGCTCTGA GACGGTAAGA AACCAGCCTG 660
AGTCATATGG CTACCAAGTT GTGGAACTTG ATTTAAACCC ACAACTGACT GTCTCCAAAA 720
GCTTTAAAAA AAACAGTGTC TTGGCCTCAC CCTCAGAAGT GCTTCTCTTT TTCTTTTGGA 780
GTGGGCCTCA GCCATCAGCA TGTTTTAAAA GCTTCCTGGG TAATTCTGCT ATGTAGCCAG 840
AGTTGAGAAT TGCTGCTCTG TGCTATGCTA ATGGGAAAGG TGGGCCTCAG TTTCCCCATA 900
TGTAAAATAA AGATATTGGG CAATATGTCC CTTTATTCCA TTTCCAGTCC TCAGTGGTTC 960
TGAGGATTTG TGGCTTGACT TTCTTACATC TCTGTACACA CACAAACACA CACACACATA 1020
CCCCTAAGCT CTGTCAGAGT CAGGACTGAG GATATGAGGA CCTTTGTCCA GGATGGGCCC 1080
CAGCCACTGG ACTGTCAACC TCTGCAGGCA CAACCCCTGT GGACATAGCC TCTCAGAAGA 1140
GCCAGACACT TCTATTTCTG CCCTAATGGG CATGATTGGA AATTTTCCCC AAGCAGCTGG 1200
AAAATAATCC TAAAATAACA GAAGTGGAAA AGCAGATAGC TCTGAATTGT CCAGGCCAAA 1260
AATGAATAGT AAAAACAAAA CCCCTTATGG TGCATTTAGC TTTGGATAAA AATCCAAATG 1320
TATTTATTTG GAGAGGAAGA GGGGAGCGTG GTGGCTGCAT AATTCTCTCC CTAAGCATAT 1380
TCTGTCCCAG CTGTTAGTGA AATAAGTTGG TCTTTCCAAA ACTCACCTTG GCTGAAGATA 1440
GACAGGAAGA GGGTCTGCAG ACTGGCGGTA CCATTTCCTG GATTGCGTTA ATTTACCATG 1500
AAACTCACCC TCTTGCAAGC CTCTTAGGGA CTGGGAAAGA CCCCCAGGGC ACTGATGCTA 1560
CAAGAGTATC TTCTAGAAGA AAGGAGTCTT GGAATTGTTC AGCCTACCTC CCTTGCTATA 1620
GACTGGAAAA AGCCAGCTCA GAAAGGGGAA GTGACTTGCT TAAGGACACA GAGCAAACCA 1680
ATGTCAGAAC TAGGAAGGAC ACAAGTGTCT GACCCTCAGC CCGTTGCTCT TACCATTGCC 1740
CGCTGTTTTT TTGGTGGGGG CTTGCATGGG GGAATCCTAA ATCATCAAAG AAAATCGAAC 1800
TCTCACAGTG GCAAGAGCCC AGCAGTTTGT ACAATTGATG GAAGAGGATT TTTCTGCTTT 1860
CTGAGGGTCC CTAATGCAAT GCAGTGAGGG ATGAAAAATG GAGGAAACGC GCACACACAC 1920
GCGCGCGCGC AGGAACAGCT GACTCAGCAA GGCCCCAGAC CAGGCTTGTT CCCAGAGAGG 1980
AGAGAGGTTG AGTAAGGACA CTGGGCCTAG GAAGCTTTGT TAGTGGCTAA TCAGGGAAGG 2040
CTTTCAGGAG CAGTGGCAGA TGGAGGGCCC TACCGTGGGC ATGAATGTGA ACTGTTCTGT 2100
TTGTAGGAAA CCCAGGCAGC CCCCTGTGAG TGTCCTGGAG GTGGACAAAG GTGGCCCCGG 2160
CACTGGCACT TGTCTCCCTG TGTTCCCTCA CTGCTCCACC TGGCTCATCT GCTCTGCCTG 2220
GCTTATCTTC CCATCGAGGT TGAGCTCTGA AGTCTGGAGC TGCCCATCAG GATGCCTTTC 2280
CCTGTCCAGG GTGCCCCATG TCCTGCCCTA TTGCCCTTTT GATTCATGGA GCCATCCATG 2340
AACACTGACA TCAGGAATGC TAGGAGCTTT GTGACATTCG TTCTCAGGGC CAGGAGGCAG 2400
GTAGAGGGGG TCTGGGGAAG GAAGTGTTAC CAGAAAGGGG TCCCAAGCCA GACCCTAGGG 2460
AAGGGTTCTT GGACCTCAGG CAAGAAAGAA ACAGGGGCAA GTCCACAAAG TAAAGTGAAA 2520
GCAAGTTTAT TAGGAAAGTA AGGGGATAAA GAATAGCTAC TCCATGGGCA GAGCAGCAGC 2580
ATGGGCTGCT CGAATGAATA TACTTAGAGT TATTTCTTGA TCAAACAAGG GGTGGATTAT 2640
TCATGAGTTT TCTGGGAAAG GGGTAGGCAT TTCCTGGAGC TAAGGGTTTC CCCGCTTTTT 2700
AGACTATATA GGGTAACTTC TTTACTGCCA TGGCATTTGT AAACTGTCTT GGCGCTGGTG 2760
GGAGTGTCTT TTAGCTTACT AATGCATTAT AATTAGCACA TAATGAGCAG TGAGGATGAC 2820
CAGAGGCCAC TTTCATTGCC ATCTTGGTTT TGGTGGGTTT GGGCCGGCTT CTTTACCACA 2880
TCTTGTTTTA TCAGCAGGGT CTTTGTGACC TGTATCTTGT GCTGACCTCC TGTCTTATCC 2940
TGTGACTAAG AATGCCTAAC CTCCTGGGAA TGCAGCCCAG CCGGTCTCAG CTGCCCCAGC 3000
CCCTATTTAA GATGGAGCTG CTCTTGAGCT GTAAGAAAGT TGCTCTGGAG CTGTAAGAAA 3060
GTCAAGATGG ATCACCTCTG ACAGAAGTAT GACATATTGA CTGCTTACTA TGTAGCAGGC 3120
ACTCTGCTAA TACCACCTGT GCAGCCTTTT CAATGATCCT TTGAGGCACT GGGTTGGTGG 3180
TGAATGCTTT AAACTTCAAG TAACAGCAAG CCCGGCTATG GTAGCTTCAG CCATAAGGAT 3240
GCTATTGTTC GTCTAGTGGG AAGTCTGGAA GTTGGGGTCC AGGGCTAGTT TAGCAGCTCT 3300
TTGATGCCTT CAGTTCCCAC TGTGTTCCCT CACTACTCCA CCTGGGCTTC TCTCTACCCT 3360
TCTATTCCTC CATCTTCAAG TGGTTGGCTT TTTGTCCTCA GGTTTCTCAC CTCATGGTTG 3420
CAAAATGGCA GCTGCAGCTC CAGACACCTC ACCCATTCGA AGGCAAGAGG TCACAGGCAA 3480
ATGGCTTTCT CCTCCTAGGC TCTGCATTAT TGTTAGGGAA CACATATTGT TCCAAATGCT 3540
TTATTGACCA CCCGTGATGT GATGAAGGCT AGGAAAGGGG GTGAATGGCC AAGGAGAGCA 3600
GGATGGTCAA GATCGGCTCT GACCAAATGT GATACATCTC CTGAGTCAGG GCACATTGCC 3660
GCCAGAGCCA GAATCAGGGT CTGTTAGCAA GGAGGGGGAG AGGGGACTGG TTCCTGGGGA 3720
GCTAACTCAG TAAGTATCAT AGGCAGGGAC TATTATGACC CCATTTCACA GAAAAAGAAG 3780
CCGCCCAGAA AGCTCAGATA GCTCCAAGTG GCTAACTAAG GACTAAACTT GGAAGGTTTG 3840
GCTCCAGAGC ATGCGGGCAG AAGGTCTTAC ATGAAAGGGT TCAAGGCCCA ACACTCTGGA 3900
CCTGCCGCTT GAATGCCCAT CCCCTTTCCC GTCTCCTTAC CAACCTGCAC CTCACACTAT 3960
TTTCTCATCT GCATGGAGGG TGTGATATTC AGAGCCTCAG GGAAGGAGCT GTTGCAGGTA 4020
TCTAAAATCC CTAGCCTGGT GCCTGCCATG GAGTATATGC TTATTTAACA CCAGTGGGTT 4080
GGTTGGGCTA GAGGTTATGT ATTGTAGTGG TCACAAACGT GGCCTGGAGG TCACGTGTCT 4140
TGCATTCTTG TTCTGGCTCT GACACTAATA AGTGATGTGA CCTCAGGAGG TCATTTTACT 4200
TCTCTGGGTT TCTTTGGCTG TAGAGTGAGG GGCTGGACCA CATCACTAGC TTTGAAACTT 4260
TCCCACTGAG CTATGTGTAT TCGTCAGCAA TGCCTGATGG AAGAGAGTAG GGGGATACCC 4320
AAAGGTGGAG GCCACATGTC CGTATACCTC ATGGCTATAC CATTACCTAC TTTACATAAC 4380
AAACCAACAT TCAGTGGCTT TCAACAGTCA CTATTTTATA TTTGCTCACA ATTCTATGGC 4440
TCAGCAATTT GGGCTGGGTT CAGCTGAGTG GTTCTTCTGT TGGTCTTTTC TGGGGTCAGT 4500
CATGCAGCTG CAATCATCTA GCAACTTGAC TAGAGGGGGA TGGTCTATGA TGGCCTCACT 4560
CATGTGTCTT GTGTTGGGTG CTGGCTGTTG GCTGGGCCAC ACAACTCCAG 4610
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