| Tag | Content |
|---|
EnhancerAtlas ID | HS049-05727 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr3:128771580-128772890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr3:128772264-128772275 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr3:128772264-128772275 | TTTCTGGGAAA | + | 6.32 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23486 | chr3:128770602-128773215 | Colon_Crypt_1 | | SE_24156 | chr3:128771502-128772247 | Colon_Crypt_2 | | SE_24156 | chr3:128772283-128773163 | Colon_Crypt_2 | | SE_53691 | chr3:128771649-128772871 | Spleen |
|
| | 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 |
| GH03I129050 | chr3 | 128769817 | 128774476 |
|
Enhancer Sequence | GCTCCATCAG AGCATAGGGG CTACGCACAT ATGTCTGTGG CAGATTCTCG CAGTCCTCCA 60
CGCTACCCAC TGAGCTGTCA CAGGGAGCGC TGTGGCAGGC TTGTATGTTT ACCAGTAACC 120
ATTGGAGCCC TGACAATAAT CACTAGCAGG TTGGAAGGAG TACAAGGGTT CCCAGGCATG 180
GAGCCAGCTG AAGGGGCACT CGTGGATGCA GAGATACAGG GGTCAGGGGA GTGCATACTT 240
TTTCAGGCCC TGGGGTGGGG GTGAGGGGAT AGGGTGCAGG GGCCCAGATA GTCAAAAGGC 300
AAGGAGGTGC TGGGAGGGGC ACCGCTTGTG GCCCAGGCTC CAAGTCCCCC ATGCATGCCT 360
ACAGTCCCAT CAGACTTCCC TTACAAAATA CAAATTTAAA GATAAAATTG TTATGAATTT 420
CAAGACAGCA GCCACAGAGC TTACAACCCC AGGCACAGGG CCCTTCTGAG CAGGGAGTCC 480
CCTGCAGCTA CCCCAGCCCC ATGCCCACAA AGCCAGGCCT AGATGCATAG AGAGGCGGAG 540
AGGGGCAGTC ATCCTACAAG GTTTCAAAAA ATAGGAGAAT CGAACATTTA TGCATAGACT 600
TCACATCTTC CACTCTCCTT TAGCCTTTTT TCTATAAGAG CTTCTTTGGG ATTGTTCAGA 660
TGGCCTGCAA CACATTAAAA ATGTTTTCTG GGAAATTCTA ACTAATGTCC TCTCTCTCAA 720
CTTCTGGCAA AAAAAAGAAA ATCATTCCAT TGACCTTAAT TTGCTCTCCC CACGGCAAAA 780
AATGTCCTGT AATTTCACAC TGTTTCCACT GGGTGGCAAA TGCTGTCCCT GAGAGGAAAA 840
ATGAATGGTA AACGGTTCCA AAGCGCCTCC AAGCATGAGC TCCGGGAGTC CAAGTTTAAC 900
TTCTCCGAAT GAACCCCTGC CCCCTCACGG CCCCTGCCGT GGGTATTTGC CACATCTTCC 960
CATCATCTGT GCTATTACCT GTGTTAAAAC ACACACACAC ACACACACAC ACACACACAC 1020
ACACACACAC ACACACACGT ATACATTTAG AAGAAGAGAA GCCTTTATTT CCTGTAAAAG 1080
GTGCCAGCCT ACAAGGTGGC CATCTGCAGG CTGGGAAGTG TGCCAATGGC CGAGCACTTT 1140
GAAAGAGGAG GGGTTGGGGC AGGAGCTTTA TGCTGACCTG TCTGGCTAAA CATACATATT 1200
CAACTGGCTA CAGGAGGAGC TATGAATATT CATAAAGGCA CTGTGCCTCC TATCTGTAAT 1260
CCTAGCATTT TGGGAGGCTG AGGCAGGAGG ATTGTTTGAG CCCAGGAGCT 1310
|
