| Tag | Content |
|---|
EnhancerAtlas ID | HS082-03038 | Organism | Homo sapiens | Tissue/cell | HCASMC | Coordinate | chr1:212352350-212353530 | 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 | TCCTGTCTTC AGCTCTACTA TTGGTGGTCT GGGCCCTGGC TGAGCACCAC AACCTATACA 60
GATCATGCTC AAGGCAGGAA GTCAAGGCTT CACTCTGTCA CTACATTTCT TGCTGCTTAG 120
CATTTGTGTA TTTTCGACAT ATGTTTTTCC AGTCTCCCAT TAAATTAGAA TCACAGAATG 180
TTAGGAATGG AAAGAACTTA AGAGCCCTTT AGTTCATGGA GCAGCTCCAC AGCCTGTTCC 240
CAAACACCTC TAGGGGCTTT GGCATTTGAC CCAGAACTCC CCTCACATTA CAGCAGCAGT 300
TCCCAGCGGG TAGGAGCTTT CCCTTGTACT TCTGCCTCAT TGCCTCCACA ACTGACGCAA 360
GGATCTCCAA AATCAGGGTT CAGTGTTGTT GACAAGGGGA GCAGAATTTT CTAGCTCCAA 420
GCACCCTCAA AGGTCCTCTT TGTTTTGCCA ACAGTCCTGC AGGTACAGGC ATAGCTGCTT 480
TGCCCCACTT TGGTGGTGCT GAGGAATGGC AGGCATGACT ACTCTAAGGC TGAGGTCAAG 540
CCACCCATCC TGCCTCTGAT CCCTGTCCCC CATGCCACCA CCCCAGCCTG GTGCCCTCTC 600
TACCCTAGAC TAAGCTGTCT CTATTCTGTG AGCATGAGAG GAGGAACTGT AGTATAGGAT 660
AGTGTAGTGT AAAGACTCTT CTATATCCCT TCCTGGGCAA GTCTTGCCCC CACATGTTCC 720
AGCCTGGGAA TCTCAGCACG GCATTTGTGT TCACTGCTGG CTTGGGTTGG GAACCGTAAT 780
CACACCCTGA TGAGGATTAA TAAGCTTCCT GGGCCTGTTG GGTGACTGTG CCTCAGAAAC 840
TGTCCAATCC AGAGCTGGGT CTATCCCCAT AGCACAGCAT GCTTTGCTAT GAGTCAGAGC 900
TTTGCAAATG CTGAAATTAC CACCACCATG TTCCTAGGGA TGACACATAC TCCCAAATGC 960
CATCACTATA TATTTTCTTC CACAGTAAGC CTTATAGCTG GTCTGCAGGT TGGCTTAAAT 1020
TTTGGTTAAG TTTCTTTTTG TCTCAGTTCT CAATTATTCC TGCTAGGGGA AGCAGTGGTC 1080
ATTTGGATAA TCCAAAAGGA TGGATTATCT AAAAATAATT TGAATTTATC TCTGGAATGT 1140
GTTAGGTGAT TTATTTGTTT TAAGCACAGC AGTTACCTTT 1180
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