| Tag | Content |
|---|
EnhancerAtlas ID | HS146-01269 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr1:212352260-212353340 | 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 | CTCTTTTACA ACAGCTCTCT GAACTTTCAA CTAGACTCAC TGTCTTTTCT CATACTCACG 60
CCCTTCATCC CATGTCCAGC CTCACTGTCT TCCTGTCTTC AGCTCTACTA TTGGTGGTCT 120
GGGCCCTGGC TGAGCACCAC AACCTATACA GATCATGCTC AAGGCAGGAA GTCAAGGCTT 180
CACTCTGTCA CTACATTTCT TGCTGCTTAG CATTTGTGTA TTTTCGACAT ATGTTTTTCC 240
AGTCTCCCAT TAAATTAGAA TCACAGAATG TTAGGAATGG AAAGAACTTA AGAGCCCTTT 300
AGTTCATGGA GCAGCTCCAC AGCCTGTTCC CAAACACCTC TAGGGGCTTT GGCATTTGAC 360
CCAGAACTCC CCTCACATTA CAGCAGCAGT TCCCAGCGGG TAGGAGCTTT CCCTTGTACT 420
TCTGCCTCAT TGCCTCCACA ACTGACGCAA GGATCTCCAA AATCAGGGTT CAGTGTTGTT 480
GACAAGGGGA GCAGAATTTT CTAGCTCCAA GCACCCTCAA AGGTCCTCTT TGTTTTGCCA 540
ACAGTCCTGC AGGTACAGGC ATAGCTGCTT TGCCCCACTT TGGTGGTGCT GAGGAATGGC 600
AGGCATGACT ACTCTAAGGC TGAGGTCAAG CCACCCATCC TGCCTCTGAT CCCTGTCCCC 660
CATGCCACCA CCCCAGCCTG GTGCCCTCTC TACCCTAGAC TAAGCTGTCT CTATTCTGTG 720
AGCATGAGAG GAGGAACTGT AGTATAGGAT AGTGTAGTGT AAAGACTCTT CTATATCCCT 780
TCCTGGGCAA GTCTTGCCCC CACATGTTCC AGCCTGGGAA TCTCAGCACG GCATTTGTGT 840
TCACTGCTGG CTTGGGTTGG GAACCGTAAT CACACCCTGA TGAGGATTAA TAAGCTTCCT 900
GGGCCTGTTG GGTGACTGTG CCTCAGAAAC TGTCCAATCC AGAGCTGGGT CTATCCCCAT 960
AGCACAGCAT GCTTTGCTAT GAGTCAGAGC TTTGCAAATG CTGAAATTAC CACCACCATG 1020
TTCCTAGGGA TGACACATAC TCCCAAATGC CATCACTATA TATTTTCTTC CACAGTAAGC 1080
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