| Tag | Content |
|---|
EnhancerAtlas ID | HS139-04658 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr1:212351900-212353650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr1:212352485-212352495 | GACATATGTT | - | 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 |
| GH01I212178 | chr1 | 212352243 | 212353985 |
| Enhancer Sequence | TCTTCCCTTG AGACATTTAC TGAGCAGTCA CAAAAGTATC TTCAGTCCAT CCACATGACA 60
ATTGCTTAGG TGTTTGCAGG AGAGGAACCC ATCTCAGGTT TTTGATCCAC AGGAGGCAGG 120
GTCCTGAGAT GCCTCAGTCA CTGCAGACAA GGCCCAAAGA AGCCCCGAAT CCTCTGCACC 180
CACCTCCCTC TCACCAAAAA CCCTTTTCGG GGGAAGAGTG GAATCATCTT ACACGAGAAG 240
AACTTAATAT CTCAAATGAA ACAACAGCCA AGTTTCTCTT CTCCAGGAGA AAAGAGATTT 300
CCAGACTCTG AGTTAAAAAA AAAAAAAAGA AGTCATTTTT TGGAGTTTCC TCTTTCCAAT 360
CTCTTTTACA ACAGCTCTCT GAACTTTCAA CTAGACTCAC TGTCTTTTCT CATACTCACG 420
CCCTTCATCC CATGTCCAGC CTCACTGTCT TCCTGTCTTC AGCTCTACTA TTGGTGGTCT 480
GGGCCCTGGC TGAGCACCAC AACCTATACA GATCATGCTC AAGGCAGGAA GTCAAGGCTT 540
CACTCTGTCA CTACATTTCT TGCTGCTTAG CATTTGTGTA TTTTCGACAT ATGTTTTTCC 600
AGTCTCCCAT TAAATTAGAA TCACAGAATG TTAGGAATGG AAAGAACTTA AGAGCCCTTT 660
AGTTCATGGA GCAGCTCCAC AGCCTGTTCC CAAACACCTC TAGGGGCTTT GGCATTTGAC 720
CCAGAACTCC CCTCACATTA CAGCAGCAGT TCCCAGCGGG TAGGAGCTTT CCCTTGTACT 780
TCTGCCTCAT TGCCTCCACA ACTGACGCAA GGATCTCCAA AATCAGGGTT CAGTGTTGTT 840
GACAAGGGGA GCAGAATTTT CTAGCTCCAA GCACCCTCAA AGGTCCTCTT TGTTTTGCCA 900
ACAGTCCTGC AGGTACAGGC ATAGCTGCTT TGCCCCACTT TGGTGGTGCT GAGGAATGGC 960
AGGCATGACT ACTCTAAGGC TGAGGTCAAG CCACCCATCC TGCCTCTGAT CCCTGTCCCC 1020
CATGCCACCA CCCCAGCCTG GTGCCCTCTC TACCCTAGAC TAAGCTGTCT CTATTCTGTG 1080
AGCATGAGAG GAGGAACTGT AGTATAGGAT AGTGTAGTGT AAAGACTCTT CTATATCCCT 1140
TCCTGGGCAA GTCTTGCCCC CACATGTTCC AGCCTGGGAA TCTCAGCACG GCATTTGTGT 1200
TCACTGCTGG CTTGGGTTGG GAACCGTAAT CACACCCTGA TGAGGATTAA TAAGCTTCCT 1260
GGGCCTGTTG GGTGACTGTG CCTCAGAAAC TGTCCAATCC AGAGCTGGGT CTATCCCCAT 1320
AGCACAGCAT GCTTTGCTAT GAGTCAGAGC TTTGCAAATG CTGAAATTAC CACCACCATG 1380
TTCCTAGGGA TGACACATAC TCCCAAATGC CATCACTATA TATTTTCTTC CACAGTAAGC 1440
CTTATAGCTG GTCTGCAGGT TGGCTTAAAT TTTGGTTAAG TTTCTTTTTG TCTCAGTTCT 1500
CAATTATTCC TGCTAGGGGA AGCAGTGGTC ATTTGGATAA TCCAAAAGGA TGGATTATCT 1560
AAAAATAATT TGAATTTATC TCTGGAATGT GTTAGGTGAT TTATTTGTTT TAAGCACAGC 1620
AGTTACCTTT CTAATGATAC TTAATCAGGG TAATGTGAAA GAAATAGCAT TCCATCACCA 1680
CAGATGAGTT AGATAGGCAG TTCTGGAGGT TGGGGAGAGA GGAGCAAGTG AGGCAGGGTT 1740
ACGAAACAAC 1750
|
| |
|
|
|
