| Tag | Content |
|---|
EnhancerAtlas ID | HS196-29994 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr7:139938450-139939780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr7:139939564-139939582 | GGAGGGAGAGAAGGAGGG | + | 6.03 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23582 | chr7:139937332-139939898 | Colon_Crypt_1 | | SE_23882 | chr7:139937414-139939930 | Colon_Crypt_2 | | SE_32404 | chr7:139938179-139939876 | Gastric | | SE_50458 | chr7:139937333-139940083 | Sigmoid_Colon | | SE_52813 | chr7:139937328-139939997 | Small_Intestine | | SE_63142 | chr7:139906757-139942538 | Tonsil |
|
| | 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 |
| GH07I140238 | chr7 | 139938054 | 139939943 |
|
Enhancer Sequence | TCCTTCCTGT GGGGTTCCTG GGGATTGGCA CACACAGAGG ATAAAGGCAA ATGGCACAGA 60
GCCTGACACT CCACTCGGGG CAGGGCTCTG GGCTGCATGG CACAGCTGAG GCTCGGAACT 120
CCAGGATCCA GAGGTTCTCC CTTCCCTGGC CATGCTTGGG CCCAACCTGC CAGTGCTCAT 180
GTGGGGAGGA TGAGGGAGGC CAGAAGGACA GGCTCCAAGA GGACCTTGGT TCGCCGTCCT 240
TGTTCTGTCC CCAGAGCTGG AGGAGCCAGT GAGAAGAGCA AGATCCATCC ACCCCCTGAG 300
AGTAGGATGT GGGAGGGAAG GCCACACCTT GGCACAGACC TCATCACACA GGGTCCCCGC 360
CCCCTTATAC AGGTGGCTGA AGCAGAGTCC TGGATCCTGG CCAAAGGGAT TGGCAGCAGC 420
TCCCTAGAGG GAAGCCAGCC AGGGGCGGGC TTCTTGTCCC CTACGGGAAC ATGGTCTCAT 480
TTGATCTTCA CAGCCTCCCT GTTTTACAGA TGGGGAAACT GAACTGCATG CTAAACAAGG 540
ATGAGGAATT GGGTCTAGGT CACGCAGGTA GTAAGCAGAG CTGGGCTTTG ATGCTGTGGC 600
CGACTCTGCA GCCTCTGCCC AGGTTCTTCT TTGGGATACA ACTGCTGACA GCTCACCGCC 660
AGTCTGTTCC CAGGAATAGC CCTGCCTGAA GGGGGCTGCC TGGCCCAAGG GTGGCTCCTT 720
CCTTGCGGGG CAGCCTGAAT TCAACCGAAC CATGTAGGGG TGAGATATGG GGAGTGGGGT 780
GCAAAAACCC AGCCCCTTGC CTCCACTCAG GACAACTCCG AAGGGCTTTG TAACTCGTCA 840
TGGGATGGAG GGCCGGGCTT TGGTGGCAAG TGCATCACAT TTCACCTTCT CCCTTGGCCC 900
AGCCCTGCTC TCCTCTTACA GTTGCTGTGC TGAGCACATG CCTGGATCAG CCTCTGCGGG 960
CATCTTGCCT ATGCCATCTG CACTCCCCGT CCTTAGGAAG TGCTGCCTCA CCTCCTTCCT 1020
AGGACCCAGG ACAAATAAAC CAAAGATCCA AAAAGTAGAG GGTGAGGCAG CCCAGAGGTT 1080
TACAACAGCA GTAAGTGACT GCCACCCCTA GGCTGGAGGG AGAGAAGGAG GGGGCGGGGT 1140
GCCTGTGTCT AGAAGTTGGT CTTCTGCATT TCAGCAGTGC TTAGTGATCT CTCTAGGCCC 1200
CTAGCCAGTC CAGGATTCTA TGAATGGGGA CAGAAGGAGG GGTCGGGCTT CCCTGCACCC 1260
AGGGATCACC CAGCAAAGCC AGAGCTATGG TGGGTTTGTC AAGGGGGGAA ATGCAGCCCT 1320
TGATGGAAAC 1330
|
