| Tag | Content |
|---|
EnhancerAtlas ID | HS098-31184 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:112374990-112376990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr2:112376955-112376965 | TTCAAGTGGT | - | 6.02 |
|
| | 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 |
| GH02I111616 | chr2 | 112374341 | 112377462 |
|
Enhancer Sequence | GGGAAAACAG TGGAGAGGGC ACTGAGGGTG CCCTTTTGTG GTAGAAATTG ATTTTGCAGC 60
CCTCCCCTCC CCCCCATACA CACGCACATA CACACACTGG GTATTTTGTT AGTCTTAACC 120
AAAGATCAAA ACAACATAGC CTTGACCTTA ACTCACAAAC AGCCTCCAGC TACAGGGAAA 180
AAGTCTCTGA GCAGGGGGAG TACAAGTCCC ACCAGAGCCC TTATTGATGG CAATTTAACA 240
ACAGGTATTT TATTTAAGGC CTGCATTTTT CATACAGAGA CACAGTGACT CGGCTTTCAG 300
GTATGTCTCA TAAGGAAGTA GGAATGGAGA AAAGACTTGG GATTTTGAAT ATTTTACACA 360
GCTTTACTGA TGAACAGTAA ACTGGAAGTG ATCGCCATGT CTGACTGTAA AGGAATAGTT 420
AAATAAATGT GCCACCCATG AGTAGAATGC ATACCTTACG CACGTGTGCA TGCACCTTCT 480
CCAGGCAGGA AGAGTTTCCT GTGCACCCCT CACCTCCACC CATAGGAAGA GCTATGGGAC 540
CTACAGGAAC TCCAGTGCTC CTGGGGCACT CCCAGCCTGT GGCACTGGAG TGTCACGTGG 600
ACAACAGAGG GTGGCTTTGT GGTCAGAACA GCATGGGCTC AAATCCAGCT TGGTCTTGCC 660
TTGGCCTGCG TAGCCCGGGC AGCTCTTCTG CCTCCCCCAA CCCAGGGAAG TGGGGTTGAT 720
GTTCTGAATC TGCAGGGCTC TTGGAGAAGT TACAGGGTGC CTGACACATG GGAGCCAGGC 780
TCTGCCCACA GTCACCCAGC CAGCATGTTG CAGAGCCAGG ATTTTAAATT AGATCCAGCC 840
AGTTCCAGAA TCATTACTTT TTCCGTTCCG TATGCATACC AGGCTGCCTC TTTCTAGATT 900
ATCCTCCAAA AAGCCCTGGG GAGGCGGCAG CAGCATGAGC GGCAGACAGG CGGCCAAGAA 960
GTGAGGCCCC AGACAGGGAT CTGAGCGTGA TCTTTGCCCT TGGGACGCAA GGCATCCATC 1020
CAAGAGGTCA CAGAAATCAG CAGCTTTCAC CGGGAAGCCC CAAGTCCTGG GATTGGGGTG 1080
CTGAAGGGGG ATCCAAAAAA AACAGTCATT GATTTGGAAG GAGATGCTGT TCTCCATCTC 1140
AGCCAGCTGT TAAAGGGACA TGGATTGAAC TCCCAGGCAG GGAGGGGCAT TTTGTTTCCC 1200
TTGGCCACAT CAGCATGTTT TTACAGTTGA GAGAGCAGGA GATGACTCTC CAGCCTGTGG 1260
CAGAGAGAAA GTGCCCTTGG CCCAACTCCG TGGAAGATGT TCCCCACCCC CCTTCCAGGA 1320
GAAGCTCCTG CTGGTGGATG CACGAACCCA GCTGGTGGCG ACACAAGGCC AGTGGGCACT 1380
CTCTGCCTTG CTGAGGCCTC AGCCTCCTGG CTGCGAAGGC CCCGGGTTCC CCTCTGCAGC 1440
CAAGTCTTTA CTTCCCCTTC ACCCTGAAAA ACGTCTTCAC AGACTATCAT TCTTGGTCTC 1500
TTGACTGCCT TTCTCCGGTT TCCTTTCACA ATCCCTCAGA GATGGGACAT CTCTCCAGAG 1560
GACGCCTGGG TTGTGAGGAT CTATGGTCAG AACATTTTGG TCAATGACAG ATTACATACA 1620
CCACAGTGGC TCCCTCAGAT TATAAAGGAG CTGAATAATT CCTATCACCA AGTGACAGTG 1680
CTATGCCATC TAAGCTTGTG TAAGTACACC CTGTGATGTT CACACAATGA CGAAATCACC 1740
ATTGTTAAGT AAATGGGTTT GGGAGAAGGT TCAAACAGCT TCCACCTGCC CCACCCTTCC 1800
GTTTCCTAAG CTCAGCCATG CCTTTGGAGG GTAGCACCTT TGTTTCTTCC ACATGTCGCA 1860
AATACAGTGA CACATGACTG TATTCAGGAA CAAGGAGGCT CTGGTGCAAA AAGAACATCA 1920
TTTCCATATG TGAGTGGGTC TTCTGGGTCC ATCACAGGCA GCCAATTCAA GTGGTCCATC 1980
CGTCAACAGA ATTCTTCTTC 2000
|
