| Tag | Content |
|---|
EnhancerAtlas ID | HS052-28090 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr4:2322260-2325110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr4:2324755-2324765 | GACATATGTT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGAAAAGTGT ATCTGCACAC ATCAGTGCTG CAATCAGATA AATTAGCCTC AAGGTTTGTT 60
ACCAAAATCT ACCTTCTTGC AAGTAATAAA AACTGGATTT GTGGTTAAAT TTATCTGCAG 120
AGCTTTATGA GAACTGGACC TGGAACCATC TTCTCCAAAA GCAAAACCAG CTGGAGGTGC 180
GAGCTGAGGC CCGCACGGGT TCCCTTCCTG CAGCCTGGCC AACGCTCCAC AAGCCACGAG 240
ACCAAAGCAG CCTCCCCTCA TCCCCCACAC AGGACCCACC TCCCTTGTGG TGCCCACCAT 300
GCCCCGAGAA GCTCCCCTCC CCAGGACTGG GGCCGCATGT GGCTGAGGCC GGCTTTCCTC 360
ACTGTCCCTC CCCCAGAGTC CGGCTCAAAG CCTGCTGAAG GACAAGCTTC CCAGATGCCA 420
CCTCCAGTGG CACCCACTCC TCTCCACGCA CCGTCCAGCC CTGCCAAGCT CCGAGTGTGC 480
CTTGATCATC CATGTCTCAG CCCGTCTCTC CTTGAGGGCA CCCATCCCAG AGGACCTTCT 540
CTGGGTGCCT CCTCCTGGGT CTCTTGGGAC CAGACCATGT CTCAGGTGCC TGGGGAGCAT 600
CCACCCACGA ATTCGTCCCC TGTCCCTCAT CATATTCTTC CTCATCAGAG CACAGACAAG 660
GGCCATGTGG GCCTGTCTGT GTAAATGGAG CACCACCGGC CTGTCTCTTT CAGCAGACGT 720
GACACCAGGG TTAGGTCCAG CCAACACCGA GTCCCTGGGA GCACAGGGAC AGTCTCCTTG 780
TCTAACACAC CCAGCTCAGT GAGAAAGGCT GATGAACAGA ATTGAACAAA GGGAATGTTT 840
TTCCCTAAAA ATCGTTGGGT TTCATGTGCA AAAAGAAGAT TTGAAAGTCA CAGGAAAAGT 900
ATGTGCAGTG CTGCCTCCGG GGCCCCTGTG GAGTGGCCAG CTCAGCTGGG CAGGGGGCTG 960
TGTCTTGACC ACCTGTGGGT GAGGGGACAG CACAACCAGC CTTCCATTCT GCTTGGTCTC 1020
CTTTGTGGCT CTTACATGAG CTGCCTGTCC TGATTGAACG AACAGTATTC AGGGGACAAT 1080
TACCCAAATA GAGCCTTAAC TTTATGGGTG AATCAGGCAG TCTCAGGACA AAGGCAGAGT 1140
GAAACAGAGC AGGGAAGGGG GCAGCCCTGA CTCCAGTGGC CAAGCCTCAG GGAAGCCATC 1200
CACAACCACA GTAGAGCTCC CTCCCCTGCT GAGCATAGGA CTCAGTCCCG CAATGACCTG 1260
TGTACCCAAC GTCTGCCCCT CTGGAAACCT CGCTCCTGCC TGTGCCGGGC AGCAGCGTGG 1320
CCGAGGGAGG ACCCAGCTGC CCCCCAGGGC AGTCAGCAGG AGTGGGGGGA CAAGGCCCAC 1380
CCATGAGAGC TGCTGGCCCA GGACCTCAGA AAAGAACTCG TTCATCAGGA GGCTCAGACC 1440
CCAAGGCTGC TGCGCCACTT CCTCCTGGGA GCCTGCGGGG ACCCAAGACC CCCTGGGCTG 1500
TGTCCCCACA TCCAGCCGTG TGTTAGCTTT CGCGTGCTGG ACGCAGGGCC GTGCACTCCA 1560
CAGTGGCTGA GCCCTGCTGC TCAGCAGCTC TGCAGGTGCC CGAACGACAG AGAGAAGGCC 1620
CGTGGGACAG GAGATCAGGC CCAGGTGCTG AAGTAACGGG GTGTGGGGGC CAGAGGTGGG 1680
GAGCGGCCCC CGGGCGGCTG CCAGAGACTC AGCATTTGTC TCTGCACCTG GCCTGGCACT 1740
TGCAGGAATC CGGCTGAAGA GGCTCAGAAT GAGGCCTGGG AATGAGCTAT TGCCAGAAAC 1800
GGTGGGTCCA ATGCAGCCGC TGCCCATGGC TACAGCCCGA CAGGCCACCC AGGCCTGCGT 1860
CCATGCTGCC ATGAGCAGGG GTAAGCAGCA CCCACTGGTG AGCCTGGCAG GCTGGATCCT 1920
GGGGTCTCGG TGTGGCCAGG GGTGTGGGGG CACTGTGAGG GGCTTGGCCC AGGTCCAGCT 1980
AAGGTGAGCA GGAGAGAGGA CGCCCCGCAC AGTGGAGAAA GCTGGGCCCT GCTGGAAGTG 2040
GGGGTGGCCA GTCTTCCCTT TTCTTTTTTC AAATAAATTC ATATAACGAA CAACTGTTTT 2100
AAAGGGTATG ATTCTGAGGC ATTTTCTGCA TTCACGGTGC TGTGCACCCA TCACCTCTCT 2160
AGTTTCAAAA GGTTTTTATC ACCCCAGAAA ACACCCTTTT AATAATCACC ACTGACTTCC 2220
TCACCTCAGC CACTGGCAAT CCCTCATCTG CTTTCTGTCT CTATGAATTG GCCTATTCTG 2280
GGTGTTTCAT ATAAATGGAA TCACATAATA CGTGACCTTT GTGACCGCTT TTCACTTTGC 2340
ACCACGTTTT CAAGGCTCAC CATGCTGTGG CACGTGGCGA ATGTTCCCGC GCATACATTT 2400
CTTCATTCAC CCACGGGTGG AAGTTTGGAT TGTTTCTGCC TTTGGGCAAT TATGAATAAT 2460
GCTGCCATAA ACATTCGTGT AGAAGTTTGT TCACGGACAT ATGTTTTCAT TTCTCTTGGG 2520
TATATGCCTA GAAGGGTATG TGGTATGACC ATATGGATCA TATAATTCTA TGTTTAACTT 2580
TTTAAGGAAC CACCAACTGT TTTCCGTAGC AGCTGTGGCA TTTTACACTC CTGCCAGCAA 2640
TCCAAGGGTT CTGACTTCTC CACGCTCTCC CCACGTATTC TTTTCCATTT TTTTGATTAC 2700
AGCCATCCTG GTGGGTGTGA AGTGGCATCT CATCATGGTT TTGACTTGCA TTTCCTTAGT 2760
AACCAACGAT GTGGAGCATC TTTTCATGTG CCTGTTGGCC ATGTGTATAT CTTCTTAGAA 2820
GAAATGTCTA TTCAAGTCTT TCCTCATTTT 2850
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