| Tag | Content |
|---|
EnhancerAtlas ID | HS026-00251 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr1:11401500-11403820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr1:11402277-11402287 | GCCATATGGT | + | 6.02 | | ZNF263 | MA0528.1 | chr1:11403090-11403111 | AGAGGAGCAGGAGGGGAGGAG | + | 6.58 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAAAATTAA AAACTTAGCT GGGCATGGTG GTGTGTGGCT GTAGTCCCAG CTACTTGGGA 60
GGCTGAGACA GGGGGATTGC GTGAGTCCAG CAAGTCAAGG TTGCAGTGAG CCGTGATTGC 120
ACCATTGCAC CCCAGCCTGG GCAACTTAGA GTGAGACTCC ATCTCTTTTT AAAAAAAAGT 180
GAGAGATAGA AGAGGCTATT TTATATAAGG TGTCCAGACA GGCTGCTCTG ATAATATTTC 240
AGCAGAAACT TTCATGAAGT GAAGGAGTGA GCTGATAGGG GATATAAGGG TGGAGCATGC 300
AGGCAGTGGG AACAGTGATT GCAAAGGCCC TGAGGCAGGT GAGTGTGGTT GGATTGGAGC 360
CCAGGTGGGG AGAGTGGGCG GAGAAGCCAT TGAAGAGGAA ACACATAGTT CATTGTAAAG 420
GCTTATCTAT TGGCCCACGC GGCGCTCTTG CAGAATTTTG CTAGTGGAGT TCACCTGCCC 480
TGGGAGGCCC TTTGGTTCCA GCATCCTGGG TGAACTGGAT CTCCTGCCAC TCCTACCTGT 540
TCAGGACCTA GAGAACAGCA AGCCCGAGGC TCCATCTCCT GTTTACCGCT GGCTGTTCTG 600
CTCTGTTTCT GATCCATGGC ATGCAGCCAT GACTTTATAA CTTACAAAAT CCTTTATTGC 660
CATAAGTGGA GAGGAGTTTC ATGCATGCAA ACTTGTCCCA ACCTGGCAGC TTCATCTTCA 720
TTTTGTAAAT GTTGCAATGA AACTCCAGGA GGTTCTGTGC TTGCTGGAGG CGTATGGGCC 780
ATATGGTGTG GAGGAAGGGC TGTAGTTGAC CACTGCTTTA TAAGCAGCTT TGTAAACGTA 840
TATATTTCAA GATGACACAC ACATACACAC ACACACCCCA GTCCCAGAGT GACACAATCA 900
TAGGGCCATT GCCAGAGCAA TCATGAGTAC TGAAAAAGTG AACACATGGC CTCTGCACAC 960
CAGGTCCCAG GCCGCAGCTG TGGCAGACAT CCCTAATCAA TCACAGGACT CCTTCGTGCT 1020
GAGCCCAGAT GCAACCTCAG AATCCTGGAA AGCCCATATG GGGTTGATTT ATAAAAGGAA 1080
GCATTGGCCA TTTTTGCTGC AGGGGCAAGC TGTCCTGGGG GGCCTTTCCT GGGGGATAGG 1140
GAACAGCATT GGCCTAATCT CGGGTCTTGG AACCCTGTTC TTGAACCCTT GGCAGCATTC 1200
TCTGCCGGAT TTATAAAGTG ACTGCAGCTC TGGAACATGA GACAAAATTA GTGCAGCCTC 1260
AGAGAGCGCT GTCTCGAAAT TGGCTTTCCA GCGAGCGGCT GGGTCTCCTA CTCTCCCCAC 1320
AGGTGGGGCT GTTTGAGTCC CTGGTAGGAT TTGTTCCAGC TGCCAGACAT GGATTAGGCT 1380
TTTGACTGTT GAACCCAGAC AAGGGGACCA GCTGTTTAAT GAGCTGGAGG AGGAAGTGGC 1440
TCCTGAAAGC AAGTCCTTTT CTTGGCTCAG GCATGCAGAT CAGACATGGA ACCAGGAAAG 1500
CTGCCTCGCC AAGCTTGGTA ACCAGAGGGA AATGAATGAT AGTGATCTGA CAGGGAAGGA 1560
TAAGGACAGG GGAGAAGAGG GGAGGTGGGG AGAGGAGCAG GAGGGGAGGA GCCAGGAGGG 1620
AAATCATGGA CCAGCCTTTG CCTAGACCCC AGGGCTCTGC TGCAGGCTCC ACTCCTCTTG 1680
GCTTCTTTTG CTATCAGAAT CATTGTGCCT TGGATCCTGG AGATCCCGAG GCATGTAGAT 1740
GATCTAGGGG TAGGCTAGAT ACAGATTTAC ATTGATACCT GGAGACAGGA TAACCTGGGT 1800
TCAAATTCCT GTTCCTCATT GACTTGCCTC CGTTTCCTCA TCTACAAAAT GGGCTTCGTG 1860
TTTCCATGAG CAGGGGCGTA ATGCTCTCAG ACTTCCCCAC CCTGTCACAT TCTGCCATTC 1920
AGCTTTTGGT AGATGTTCAA ACTGCCATTT GGACCTTTAT CCATGGGATT TCAGTGTCTC 1980
TCTCTTGATT GGATCTGAAC TTGGTGGAGG AGGTGGTGGG TTTATTCATT AGAACCCACT 2040
GAACATTAAT GGCACCCACC CACGTGTTTG ATGTGACGAT TAAGCAGGTG AAGGTGTTTG 2100
TAGCTGCTTG TATCCTCCAT GTCTAGATAT ATAGCTAATC CATACCTGTG CATATCTATA 2160
CCTATCAATA CACACTGGGG CCCAGCACAG ATCGGTGCTT AGTTTGTTTG CTTTTTGAGA 2220
CAGTGTCTTG CTCTGTTGCC CAGGCTGGAG TGCAGCGGCA TGATCTTGGC TCACTGCAAC 2280
CTCCACCTCC CAGGTTCAAG CAATTCTCAT GCCTCAGCTT 2320
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