| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01248 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:33218780-33221510 |
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 | GCTGGTTAAA AAAATATTTA ACAGGCCGGG TGGTGTGGCT CACGCCTGTA ATCCCAGCAC 60
TTTAGGAGGC CAAAGCAGGC ATATCACCTG AGGTCAGGAG TTTGAGACCA GCCTGAACAA 120
CATGGTGAAA CCCCGTCTCT ACTAAAATTA CAAAAATTAG CCGGGCATGG TGGTGCGCAC 180
CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC GTTTGAACCG GGCAGGTGGA 240
GGTTGCAGTG AGCCGAGAGC GTGCCCCTGC CCTCCAGCCT GGGTGACAGC GAGACTTGGT 300
CTCAAAAAAA TAAAAAAAAT AATAAAAAAA GGACCTACCT TACACAATTG TGGATAAAAT 360
GAAGTAATGC ATGAAAGCGG TTAGCACAGA GCCTGGCACA TAGTAAACAC TAAGTAAAAG 420
GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT CAGTTCGATA CATTTGTACA 480
CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG 540
GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG 600
TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG 660
GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC 720
CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG 780
GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC 840
GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC 900
CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG 960
CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG 1020
CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC 1080
GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA 1140
CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG 1200
CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT 1260
CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA 1320
CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG 1380
CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC 1440
CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC 1500
GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT 1560
TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG 1620
GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA 1680
GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC 1740
GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA 1800
ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC 1860
ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG 1920
GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG 1980
AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA 2040
TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA 2100
TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC 2160
TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA 2220
CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA 2280
AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT 2340
TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG AAATCAGGGG 2400
CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC CATTTCATGG ATGACGAGAC 2460
TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC TGTGGTGGTT TGAGGTAGTA 2520
ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT CAGTTAGGCT CTTTGAGGAT 2580
TTCTCAGAAG GTAGGTGTTG ATGAGAATCT CCAGGACCTT CCAGCACTCT CCCTGCCCCA 2640
GCAGTCCTGA AAGCCCTGTC TGTGCCTACC TGTCTCTCCT AGAATCTGCA CTAAGGGGGC 2700
AGGGCTGGGG CTCTTCATCT GTCCTCTGAT 2730
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