| Tag | Content |
|---|
EnhancerAtlas ID | HS168-00117 |
Organism | Homo sapiens |
Tissue/cell | RPE |
Coordinate | chr1:33219260-33221150 |
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 | CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG 60
GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG 120
TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG 180
GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC 240
CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG 300
GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC 360
GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC 420
CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG 480
CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG 540
CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC 600
GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA 660
CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG 720
CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT 780
CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA 840
CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG 900
CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC 960
CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC 1020
GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT 1080
TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG 1140
GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA 1200
GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC 1260
GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA 1320
ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC 1380
ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG 1440
GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG 1500
AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA 1560
TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA 1620
TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC 1680
TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA 1740
CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA 1800
AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT 1860
TCCTTTCACT TGTCTGGACC ACTCTGGCTC 1890
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