| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22252 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:1084480-1085830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr7:1084970-1084984 | AGCCTTTGATCTCT | - | 6.17 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_24628 | chr7:1082971-1084736 | Colon_Crypt_2 | | SE_27490 | chr7:1082734-1085083 | Esophagus | | SE_31709 | chr7:1080404-1090350 | Gastric | | SE_41902 | chr7:1085547-1086662 | LNCaP | | SE_42709 | chr7:1082745-1097030 | Lung | | SE_47609 | chr7:1084176-1084960 | Pancreas | | SE_49104 | chr7:1082796-1085472 | Right_Atrium |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCCGCGCTCC GAGCTGAGCC CCGGGGGCGG GCTTTCGGTC ATTAACCTGG TGATGGCAGC 60
TGAATCTGCT GCTGGCGTAG GCGGCACAGC GCCGCCACCG GCTCTCCCAT GTCCGACAGG 120
GCACCACTGA TCCTGCTCTC CTGGGCCACT ATGGTGACTG CTTTCGGCCC CTTCTGTGAT 180
TAGTATTTTA AAGTGAGTTT TGGATCTGTG TCTACATGGA GGTGTCGGAT CTGCTGTCAG 240
TTGTCTTGGA CAGTTGGCAG GGCATGGGAC GGCTCTTTCA AAGCTTCACT GGAAGGCAGT 300
GCTCTCCAGC CGCCAAACCA CCACTACCAG CAGCAGAAAA CCCACTATTA AGTTAGTATT 360
ACAAACCTGG CAAGTCAGTT CTCTAAATTA GGCATAAGTC TATGAATCTT GATGTGACTG 420
GTCACAGTGG CTTATCTCTG CATGCATGCT ACGTGGTGGA CCAGAGGATA ATTCTGTATT 480
CGTCGTCCAC AGCCTTTGAT CTCTTCCCTG CCCATGAAGA TGTACTTGAG TCCTCCATTC 540
CACTTTAAAT AGCCAGCTCC TGTCCACACG GAACAGCACG ACATCTTTTA TCTTTTGCTA 600
CCTGCAGCAC CTAGCAGAGG CCAGCATTCA ATAACAGAGG GCCAAGAGGC TTGCTTTAAA 660
GGCCTCTGCA AACTTGTATG AGTAAAATGG TTCTGACCAT GTTCCCAGGC TCCTCACGCA 720
TAGTGGTGAT GAGATAGTCT ACCGTCCTAA CTGGGGCACC GTTGAGAGTG AACGGAGGCA 780
CTGTTAATAA TTAGACGAAG TGCACACTCA CAGTACCCAT GACCTGCTGT GCAGCTCCTT 840
CAAGAACTAC TGTAAGGCCT GGCTCCCCAA CCAGAACCCC TGTTGTCTTC CTCAATGAAG 900
AAGGCCTCTG AAGACAAGTG ACTTAAGAAC ATAGTTTATA TGTATTGAAT ACTGTTGTGC 960
CTTTTCACAG AGAAGAGGTC GGGGCCAGAG CAGCTCACTG CCCGACGCCA CACACATCCG 1020
TGCTGGCGTC CACGTGTCAT CCTGCCTCTC TAGCCAGCAT GGACATATCC TGAGGATGGA 1080
GGACAGAGGA ACACAGATTT AGGGCAGAAT GTAAATGTGA AAGTTGACTT GGAGTCCCTG 1140
CAACTCATAA GCCCCAGTAG GCTGATGAAG AGAGAAGGGC AAAGGGCGCG CACCTCATGT 1200
GGGTCTTAGG TTAGGATGTA AAGGCTGATT ATGTCTATCA TACAATGAAT CAATGGCATA 1260
CTGCACAGAT CGCTGCATGG GGAAATATGC TCGTGTAATT TACAGTCGGA AGAGGGACAT 1320
GCTGCTCACT GGGGCAGGGA GAAGAAGGGG 1350
|
