| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00527 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:33219160-33221220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:33219795-33219806 | GGGGGCGGGGC | - | 6.02 | | KLF16 | MA0741.1 | chr1:33219551-33219562 | GGGGGCGTGGT | - | 6.14 | | KLF5 | MA0599.1 | chr1:33219498-33219508 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:33219796-33219806 | GGGGCGGGGC | - | 6.02 | | SP1 | MA0079.4 | chr1:33219495-33219510 | CAGGCCCCGCCCCTC | + | 6.22 | | SP4 | MA0685.1 | chr1:33219495-33219512 | CAGGCCCCGCCCCTCCT | + | 6.32 | | ZNF263 | MA0528.1 | chr1:33220523-33220544 | TCCCCCCCTCCCCCGTCCCCA | - | 6.03 | | ZNF263 | MA0528.1 | chr1:33220656-33220677 | TGGGGAGGGGAGGGAAAGGGG | + | 6.2 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_00938 | chr1:33219006-33222393 | Adrenal_Gland | | SE_23116 | chr1:33219622-33222368 | Colon_Crypt_1 | | SE_23802 | chr1:33219124-33219553 | Colon_Crypt_2 | | SE_23802 | chr1:33219604-33220504 | Colon_Crypt_2 | | SE_23802 | chr1:33220519-33221309 | Colon_Crypt_2 | | SE_24863 | chr1:33219103-33221902 | Colon_Crypt_3 | | SE_26629 | chr1:33219003-33222323 | Esophagus | | SE_28121 | chr1:33220540-33221955 | Fetal_Intestine | | SE_29204 | chr1:33219822-33221616 | Fetal_Intestine_Large | | SE_31442 | chr1:33219069-33222394 | Gastric | | SE_32998 | chr1:33219539-33221354 | H1 | | SE_34017 | chr1:33218987-33219471 | HCC1954 | | SE_34017 | chr1:33219830-33221722 | HCC1954 | | SE_36587 | chr1:33219820-33221157 | HMEC | | SE_41588 | chr1:33219113-33221709 | LNCaP | | SE_47530 | chr1:33219105-33219467 | Pancreas | | SE_47530 | chr1:33219506-33221824 | Pancreas | | SE_50335 | chr1:33220528-33222187 | Sigmoid_Colon | | SE_52480 | chr1:33219537-33222050 | Small_Intestine | | SE_64801 | chr1:33219051-33219585 | NHEK | | SE_64801 | chr1:33219594-33221668 | NHEK | | SE_65538 | chr1:33218762-33221927 | Pancreatic_islets | | SE_68878 | chr1:33219160-33221410 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTAGCACAGA GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC 60
TGTAACTACA GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC 120
GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC 180
CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA 240
CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA 300
GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC 360
GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC 420
GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC 480
CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT 540
CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC 600
GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG 660
GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT 720
GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG 780
TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC 840
ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA 900
CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA 960
TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA 1020
CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG 1080
ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA 1140
CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG 1200
GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG 1260
GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC 1320
TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC 1380
CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA 1440
CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG 1500
GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC 1560
AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT 1620
AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC 1680
CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG 1740
TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG 1800
GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT 1860
CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC 1920
AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC 1980
ACTCTGGCTC CTACAGGGGT TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA 2040
CACTTACTGT TCTGGCTAGC 2060
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