| Tag | Content |
|---|
EnhancerAtlas ID | HS194-00095 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr1:33219170-33221140 |
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 | GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA 60
GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG 120
CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC 180
CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG 240
CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA 300
GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC 360
TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG 420
CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT 480
GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA 540
GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA 600
GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG 660
CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT 720
CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA 780
TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA 840
CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA 900
CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT 960
TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT 1020
CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC 1080
AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA 1140
CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT 1200
TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT 1260
GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA 1320
CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC 1380
CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT 1440
GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG 1500
AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA 1560
GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT 1620
GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG 1680
GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC 1740
CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC 1800
AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG 1860
AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG 1920
TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC 1970
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