| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17792 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:47564160-47566330 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:47564464-47564479 | TGAACTCCTGACCTT | - | 6.04 | | Nr5a2 | MA0505.1 | chr19:47564905-47564920 | GCTGGCCTTGAACGC | - | 6.67 | | RARA | MA0729.1 | chr19:47564461-47564479 | ACTTGAACTCCTGACCTT | - | 6.48 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I047062 | chr19 | 47565561 | 47565710 |
|
Enhancer Sequence | TGGGGAAGGG AGGGTGAAGA AAAAACAATA AAAGGAAAGA AAAGAAAGTA GATGGAATGA 60
TGGTTCAGAT GTAATAATTT TATTTATTTT TATTTATTTC TTTGAGACAG AGTCTTACTC 120
TGTAGTCCAG GCTGGAGTGC AGTGGTGTGA TCTCAGCTCA CTGCAGCCTC CGCCTCCTGG 180
GTTCAAGCAA TTCTCCTCCC TCAGCCTCCC AAGTAGCTGA GATTACAGGC GACTGCCACC 240
ACACCTGGCT AATTTTTGCA TTTTTAGTAG AGACAGGGTT TCACCATATT GGCCAGGCTG 300
GACTTGAACT CCTGACCTTA GGTGATCTGC CTGCCTCAGA GGTTGCAGTG AGCTGAGATC 360
GTGCCACTGC ATTCCAGCAT GGGCTACAGA GTGAGATTCC ATCTCAAAAA AAAAAAAAAA 420
AAAAAAAAAA AAGAGAGAGC AGGGTAACAG GGTTAATTGT TGTCCCCAAA AACATATTTC 480
TACATCCTAA GCCCTGGAAC CTGTAAATGA ACTAATGAAC TGTATTTGGA AACAGGGTCT 540
TTAAAAAATA TACATATATA AGCTCTCACT GTTGTCCAGG CCAGAGTGTG GTGGTGTGAT 600
CACAGCTCAC AGCAGCCTTG ACCTCCCAGG CTCAAGGGAT CCTCCTGCCT CAGCATCCCA 660
AGTAGCTGGG ACTACAGGTG CGCCCACCAC ACCCAGCTAA TTTTTCCTGT ATTTTGTAGA 720
GATGGGGTCT TCCTATGTTG CCCAGGCTGG CCTTGAACGC CTGGCATCAA GCAATCCTCC 780
TGCCTTTGCA TCCCAAATTG CTGAGATTAC AGGCGTGAGC CACCACACTT GGCTGGGAAA 840
CAGGATATTT AATGAAAGAT CTTAAGATGA GATTACTCTT GATTACTTGG TTGGGTTCTA 900
AATCCAGTGA AGAGTCTTTT TTTTTATTTG AGATGGAGTC TTGCTCTGTT GCCCAGGCTG 960
GAGTGTAGGG GCATGATCTC GGCTCACTGC AAGCTCCGCC TCCCGGCTTC ACGCCATTCT 1020
CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACAGGTGCCT GCCACCACAC CTGGCTAAAT 1080
TTGTTTTTTC TGTATTTTTA GTAAAGATGG GGTTTCACTG TGTTAGCCAG GATGGTCTGG 1140
TCTCGATCTC CTCACCTCAT GATCCGCCCA CCTCGGCCTC CAAAAGTGCT GGGATTACAG 1200
GCGTGAGCCA CCGCGCCCGA CTGAGTCTTT CTAAGAGACA GAAGACACAG ACACAGAGGA 1260
GAAAGCTCTG GGAAAAGATG GAGGCAGAGA TTGAAGCGAT GTCACCACAA GCCCAGGATT 1320
GTCCATGGCC ACCAGAAGCC AGGAGTGGAA AGCAAGGATT CTCCCTAGAG CCTCAGAGGC 1380
AGCCTGGCCC TGTGGACACC TTGATGGTGC ACTTCTGGCC TCTAGAACAA ATTTCTGTCA 1440
TGTTAAGCCG CCCAGTCTGT GGAGATACGT AGGCAGCCCT GGGGCTCTAA TACCAATGGA 1500
ATGCCAAAAT GGAATTTAGA AAATGCAACC AGCCGGCCAG GCACAGTGGC TCACACCTGT 1560
AATCCCAGCA CTTTGGGAGG CTGAGGCAGG TGGATCACCT GAGGTTGGGA GTTTGAGACC 1620
AGCCTGGCCA ACATGGCGAA ACTCCATCTC TGCTAAAAAT ACAATTAGCT GGGTGTGGTG 1680
GCAGACACCT GTAGTGCCAG TGACTCAGGA GGCTGAGGCA GGAGCATCAC TTGAACTGGG 1740
GAGGCAGAGG TTGCAGTGAG CCAAGATAGC ACCACTGCAC TCCAGCCTGG CGGACAGATT 1800
GAGACCCTGC CACAAAAAAA GAAAAGAAAA ACAAAAAACA AGAAAATACA GGAAACAGTT 1860
AACACCTGTA GAATCTGGGC AGTGGATCAG GGCAGGTACT CAAAGAGCAC CTGGCACCAG 1920
TTGTTGGTCC CAGTGTCCAG GTAACCCTGG GCTGTGGAAA GCTCGACCAC ATCCTGGTGC 1980
TGGTGGCCAT CTCTGCCCTC CCTCAGCCTC CATACCTTCC TCCAATGGAG ATGTTCCTCA 2040
GGCTCCACGC ACTTCCTGAG CGACATGGTC CACTCTTGCA GCTCTATTTT TTTTTTTTTT 2100
TTCAAGACGG CATCTTGCTC TGTCACCCAG GCTGGAGTGC AGTGGCACTG TCTCTGCCTC 2160
CTGGGTTCCA 2170
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