| Tag | Content |
|---|
EnhancerAtlas ID | HS096-00737 |
Organism | Homo sapiens |
Tissue/cell | hNCC |
Coordinate | chr3:184291750-184293610 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr3:184292620-184292635 | TGGCCTCTGCCCCCT | - | 6.05 | | PLAG1 | MA0163.1 | chr3:184292916-184292930 | GGGGCCCAAGGGTA | + | 6.08 | | RFX2 | MA0600.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | + | 6.34 | | RFX2 | MA0600.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | - | 6.49 | | RFX5 | MA0510.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | - | 6.76 | | RFX5 | MA0510.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | + | 6.85 | | SREBF1 | MA0595.1 | chr3:184292525-184292535 | GTGGGGTGAT | - | 6.02 | | ZNF263 | MA0528.1 | chr3:184293060-184293081 | TCCTCCTCTCACCCGTCCTCA | - | 6.25 |
|
| | 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 |
| GH03I184574 | chr3 | 184292122 | 184293070 |
|
Enhancer Sequence | CCTCGGCCTC CCAAAGCGTT GGGATTACAG GTGTAAGCCA CCACTCCTGG CCCTGGGCAA 60
GTTACTTAAC TGTTTGAACC TTGGTTTCCT TATGTGCAAG ATGAGGAAAA TAATAGAGGT 120
TCCTTCATAG GGCTGTAGCG AGGCTTCTTA TGTGAGCAAT GCTTTGCCCG TAGAACAGTG 180
TCTGGCACAT GGGAGCACAG CCACCAGCTA AGTGTTGGCC ATGAGTCTCC AGAGCCCTGG 240
CATCCACGAG AGCTGGGCTG TTCTGCCCTT ATTGTATACA TGAGGAGTTC AGGAAGCCTG 300
CCTCGGATGG CTTGCCAAGA CTTATGTACT AGGCTTCGGA GTTATCAAAA TTGTCCACCT 360
AGGGGGTCTC TCACTGAGCC TCACCAGTCC TTGTGAGGTA GATTCCTGCC ATCTCCCTAT 420
TTCGCCAATA AGGAAACTGA GTCTTGGAGA AGCTCTGTGC ACAGGCCTTG TAGCTAGGGA 480
ATGTGGAAGC TGGCACGGAA GCCTCCTCCT GTGCTCTGCC ATGCAGGATG GCATGCTGAG 540
GGCCCTGTCT TTCGCTCCCT CTGCCCGATT CTCTTCCTTG GGGCTTGCAG CCTACAGCTC 600
TGAGGGGTAG GTGATGACTC TTATGGCAGC CCTAGGCGTG AGAGGGGCTT GGCAGCATGA 660
AGCTGGCTGC GAGGCCATGT TGTCATGAGA AGGTGAACAG TGCCTTTCCC GGGCCCTCTC 720
CACTTCTCGA TGGGAATCTG TCCTGAGATT TCCTCTTCCT AAGTGGAGAA AGGGGGTGGG 780
GTGATGAGCC TGACAGCCTG AAGAGGGGCT AACACTCTGC AGGTCCCCGG CAGGAAATGC 840
ATGCTGGTTC CCATAGCAAC CAGGCTGGCC TGGCCTCTGC CCCCTCCCCC ACTGGCTCAA 900
AAGAGCTAGG GTGGAATATC ACCTTCGTGA GGGCAGATGA AACCCCAGAA AAGGGCAAGC 960
CCTAGCGCTG GGCGTTCTCC CCTATGGGTG TCCCCCTCCA CAGGCAGTCA TATGGAGAGG 1020
CAGTGACCCA CTTTAGTGTC TAGGAGGGTC TTGGTTTATG CCCATTATCC TAACACAGTT 1080
ATTACTAGTG CCTCCTTTGA CTTGCAAATG TTCCAGTGTG AAGAATACAC GATAAGGCTA 1140
CCATCAATCC ACAGAGCCTG TGTCCAGGGG CCCAAGGGTA GATGGCAGGA GGGAAGACTG 1200
GGGAGAAGGG ATGCTCAGGC CCTGGGCTTG CTCTGGGGTG AGTCCCCTTG TGGACACTTG 1260
AGGCCTCTGA ACTCCAGGTG ACCCCAGCCT TCCTGCCTGC TTTCTTTCTC TCCTCCTCTC 1320
ACCCGTCCTC AGCCCCCATC CCTGCCCAAG GGCAGACAGG AGCTGCTGCC TGCGCCTGGT 1380
GGGTGGGGCG AGAGCTTCAC TGTGAAGGTC CCGTCTCCTG GCTGTTCTAG GGTGTCCTTC 1440
AGGGTCCTCA GGAATGATTT TTCTGGAGCC TCGGGGAGAG GTGGGGCATC TCCACAGTGC 1500
CGGGTGCTGC TAGCCCACCG GTGGTCTCTT CTTCACCCCA CCTCTTCCTC TGTCTTTCTC 1560
TGTCTTCCCT GCCTCAACAA GCCCAGGCTG TCCAGGTGAT GGGGCTGACG TCTTCGTCCA 1620
TGAGGCCCCG GGGTAGGGGT GAGGGGGGCA GGGGCGGGGA GGAATCTGCT GACGTGGGGT 1680
TTCCATGGGG CAATAGGGCC TTTTGTAGCT GCAGCTGGAG TTAGGCAATC CCAGCATTGC 1740
CCCCACAGTC TAGGAGGTGG AGGGGCCAGA CCTAGGCTGG GGAGAAGCCA GGTTCTCATG 1800
GAGCTGCGGA GGTCTGGTGT CTGCAGGGAA GGGAGGTGAG CCCCATTCAT CCTCTTCTCT 1860
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