| Tag | Content |
|---|
EnhancerAtlas ID | HS146-09027 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr2:238508510-238509620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr2:238509550-238509564 | CTTCCAGGAAAGAG | + | 6.49 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_01566 | chr2:238504841-238510985 | Aorta | | SE_29379 | chr2:238508569-238513274 | Fetal_Intestine_Large | | SE_29932 | chr2:238508303-238509730 | Fetal_Muscle | | SE_32293 | chr2:238508253-238509814 | Gastric | | SE_36919 | chr2:238508089-238510123 | HSMMtube | | SE_40633 | chr2:238506906-238510777 | Left_Ventricle | | SE_42111 | chr2:238507966-238510809 | Lung | | SE_51094 | chr2:238507709-238510768 | Skeletal_Muscle | | SE_63809 | chr2:238508557-238509504 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 238509000 | 238509272 | | chr2 | 238508822 | 238509122 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I237599 | chr2 | 238508356 | 238513672 |
|
Enhancer Sequence | TCAGTTTCCA GCCACTCCAG CAGCCTGAAC ACCATTCCCT GAGTTCCTGG GCCTTACATT 60
CCAGCCTCCC TGCCCCGAGC AGCCTGGAGA GGGGCCTCGG AGGAAGGTCA TCTTAGCGTG 120
AATTTCATCC AGAGCAGTTC CTTTCTTTCA AGGGTCGAGT CCTCTCCATT CTTTGCTTCT 180
TTGGTCAGTT TGCTTCTTTG GCCACTGTCC AGTGTCCTTC AACGGTGCTT TACATCTTAT 240
CCAGAGTTGA TCATTTTTCT TTGCGGGAGA TTAGTTCAAT CCATGCTCCT GCAGTTCCTA 300
CTAGAACTGG AACTCTCCCG TTTTTTTTAA CATTACCTTT AGTGGTTGGC TTGTGCTTCT 360
TTAAAAGCGA AACCACGCTG CCACTGGGCC ATGTGGGGCC CTGGGATTTA TCCAGGTTAA 420
ATGCCGACTT AGAAGTTGGG AGATTGCCTC CATACACAGA CTCCTTCACA GCACGTTTTA 480
CACATGCACT CAGCCGCTCT GATTAGTAAA TCTCCTAAAA TAAGTACTGG GCTTATGTTC 540
ACTTCCGTTT TGGAAATCAG TGACTCTGCC CTCTGAGCTG CAGGCCGGTC TGTGCCTCTA 600
GCAGGAGCTG CAGTTCTGTG AATGATCCCT CTTCTCTGAA AGGCAGGCAG CCGGAGCTCT 660
GGAGCCCTCC GGGCGAACAG AACAGATTGC TGACTGTGGG GTAGGTCCCC TTCTGCTCTG 720
AGCTCAGCCT CACCACCTTG GGCAGACAGT AAACACAGTC CCGTGTGGTG TCGGCCGGCT 780
GGAGCTCATC CTACAAAAGG TGGCAGAGAT GGCGGTGCTG GTGGCTCCGT TTAACCCCAG 840
CATGAGCAGA GGTGGGAAAA TCTATGGCCC ACGGGCAGGC CTGGGGACTC CAAGCAGGTG 900
GAACAATAAC ATGAACTTGC CAAGATTGGC CAGGGCACAG CATCTCCACT AGGTCATCTC 960
ACAGATGCCC CAAATTCAGT GTGCTCCAAA CAACACCCTG GTTCTTCCCG GCCAAATGTG 1020
TTTATCCCCT AAGCTCCCTC CTTCCAGGAA AGAGAACTGT CCAGTGAGTT AGGCCAGAAA 1080
ACCTGGAGTC ATCTTAGTCT ACAATCCTTG 1110
|
