| Tag | Content |
|---|
EnhancerAtlas ID | HS148-01578 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr1:212351810-212353290 | 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 | TTTCTAGAAA ACCTTCCTGC TTGCTGGAAT CTGCTTAGCT TTAGAACACT CTAGTTACCT 60
CTCCCCTTTC CTAGCTTACC CTCCAAATGA TCTTCCCTTG AGACATTTAC TGAGCAGTCA 120
CAAAAGTATC TTCAGTCCAT CCACATGACA ATTGCTTAGG TGTTTGCAGG AGAGGAACCC 180
ATCTCAGGTT TTTGATCCAC AGGAGGCAGG GTCCTGAGAT GCCTCAGTCA CTGCAGACAA 240
GGCCCAAAGA AGCCCCGAAT CCTCTGCACC CACCTCCCTC TCACCAAAAA CCCTTTTCGG 300
GGGAAGAGTG GAATCATCTT ACACGAGAAG AACTTAATAT CTCAAATGAA ACAACAGCCA 360
AGTTTCTCTT CTCCAGGAGA AAAGAGATTT CCAGACTCTG AGTTAAAAAA AAAAAAAAGA 420
AGTCATTTTT TGGAGTTTCC TCTTTCCAAT CTCTTTTACA ACAGCTCTCT GAACTTTCAA 480
CTAGACTCAC TGTCTTTTCT CATACTCACG CCCTTCATCC CATGTCCAGC CTCACTGTCT 540
TCCTGTCTTC AGCTCTACTA TTGGTGGTCT GGGCCCTGGC TGAGCACCAC AACCTATACA 600
GATCATGCTC AAGGCAGGAA GTCAAGGCTT CACTCTGTCA CTACATTTCT TGCTGCTTAG 660
CATTTGTGTA TTTTCGACAT ATGTTTTTCC AGTCTCCCAT TAAATTAGAA TCACAGAATG 720
TTAGGAATGG AAAGAACTTA AGAGCCCTTT AGTTCATGGA GCAGCTCCAC AGCCTGTTCC 780
CAAACACCTC TAGGGGCTTT GGCATTTGAC CCAGAACTCC CCTCACATTA CAGCAGCAGT 840
TCCCAGCGGG TAGGAGCTTT CCCTTGTACT TCTGCCTCAT TGCCTCCACA ACTGACGCAA 900
GGATCTCCAA AATCAGGGTT CAGTGTTGTT GACAAGGGGA GCAGAATTTT CTAGCTCCAA 960
GCACCCTCAA AGGTCCTCTT TGTTTTGCCA ACAGTCCTGC AGGTACAGGC ATAGCTGCTT 1020
TGCCCCACTT TGGTGGTGCT GAGGAATGGC AGGCATGACT ACTCTAAGGC TGAGGTCAAG 1080
CCACCCATCC TGCCTCTGAT CCCTGTCCCC CATGCCACCA CCCCAGCCTG GTGCCCTCTC 1140
TACCCTAGAC TAAGCTGTCT CTATTCTGTG AGCATGAGAG GAGGAACTGT AGTATAGGAT 1200
AGTGTAGTGT AAAGACTCTT CTATATCCCT TCCTGGGCAA GTCTTGCCCC CACATGTTCC 1260
AGCCTGGGAA TCTCAGCACG GCATTTGTGT TCACTGCTGG CTTGGGTTGG GAACCGTAAT 1320
CACACCCTGA TGAGGATTAA TAAGCTTCCT GGGCCTGTTG GGTGACTGTG CCTCAGAAAC 1380
TGTCCAATCC AGAGCTGGGT CTATCCCCAT AGCACAGCAT GCTTTGCTAT GAGTCAGAGC 1440
TTTGCAAATG CTGAAATTAC CACCACCATG TTCCTAGGGA 1480
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