| Tag | Content |
|---|
EnhancerAtlas ID | HS049-02424 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr14:94569060-94570620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr14:94569780-94569795 | TGGCCTCTGACCTCA | - | 6.3 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 94569640 | 94569795 | | chr14 | 94570023 | 94570435 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH14I094102 | chr14 | 94569281 | 94569430 |
| Enhancer Sequence | GTGTCGGTTC TCTGTTCTTG TGGTCAGGAT AGGGTACAGC GCTGCTGCAG GACTGCTGGA 60
CAGGGAGGGA CTCAAGAGGA AGCAGCATGG GATGTCTGTG ACCGGAGCCA GGTCTGGCCC 120
CAGGCTTTCC ACTCATTCTG TGGTCCTGAG CAGGTCATGT CTGCCCTTTG AGCCTCAGTT 180
TGCTGCACTT CAGATGGGAG AGTCAGCCAG AGTAAGCGTT ATAGGATGGC GTGGCTCTTG 240
GGTCATTGCT TGAGCCATTG ACCCTCAATT ACGAAGCCCT TTGTCCTCAT GCGTGACTGA 300
TCCCTTCCTT TCCCACCCAG GACTCAGGGT GTGACTGATT ACTCTAGAAG TTTACTCTAG 360
AAGTTTACTC TACTGATTAC TCTAGAAGTT TAGCAACACT ACATTTGCCT GGCCTATGGG 420
CCTTCTCCAT ACAGGTCGAG AAGTTTCATT CCTCCAGGGA GCTCTGTCCC TCTCAGCACA 480
GAGCCCAGGC TCCTCAGGCC CCAGGTGGAC TGAGCAGAGC CTGTGAGGAT GGGCAAGGGG 540
CTGGGGCTCC TGAGAAGTAG GCCAATGCAG AATACCCATT TCCAGAGACC TCCTGTGTGC 600
CTGGCCCCAG ATCAGGTGCC AGCTGTCCTA TGCACACTGA CCTGGCATCT GCCACACGGC 660
ACCTGCCTGG CCTTGAGGAT AAGTAAACCA CACTTGACTT CTGCAAGGCC TATTTAGATG 720
TGGCCTCTGA CCTCAACGTT AGTCCCACTC TGGGCTGTTT GACCTTCACA CTTATTTTTC 780
CTTTACAGCT GCACTCCTGC AGGGCTCTCC CTGGGATGCT GGCTGAGCTG ACTCCCACAG 840
CTCCCAAAGG GGCCCCAAGG CTCCATCCCA CAGGATTGCC CTGGCTACAG AGGATCACAG 900
AGGTCCATCT CTGCCCAGGG TGCACAATGT TGGGGAAGCC AGCCCTTAAC CAATGATGTG 960
AAGGGACTTG GGGTAAATTA CAGAAACGAC CATATTCTCC GCCCTTTCAG CATGGCTGTA 1020
CAGCTCCTCC CATCAAGAGG TAGGAATTTC TTTCCCCTCC CTTTGAATCT CCTCTGGCCT 1080
GCGGAGTTGC TCTGGCCTGG CCGATAGAAC ACAGTGGAAG TGATGGCGTG CTAATCTTGA 1140
GCCTAGTCCC TAAGAAACCT TGCAGCCTTC TGCTGTATCT CCCGGACCCC ATCACTGCCA 1200
TGAGAACAAG CCAGGCTGGG CAAGCACACA AAGTCCATTC ATTCCAGACA AGACCCCAGA 1260
CATGGCAGCG AGCCCAGCCA AGTTCTGCAA AGCTGACCTG CAGCTGACTG CAGATGGATG 1320
AGGGGCCCAG CTGAGACCAG AAGAACCACC TGCCTAGATT GCTGACCCAC AGAATCATGA 1380
GCTACATAAC TTTTTTAAGC CACTAAATTG TGTGGTCACT TTTTATCCAG CCATGGGTAA 1440
CTGACAACAT AAGACAATGT GTAAAATCAC TGAAGAGGAT CAGGCTATAT GGCTCGTAGG 1500
ACAGAAAAGG AAGCGATAGA TTCTAATTGC AGCAACCTGG GAAGACTTCC CTGGAGTAAG 1560
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