| Tag | Content |
|---|
EnhancerAtlas ID | HS023-00698 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr1:33218470-33221220 |
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 | TGCCTGGCGT TTTTAAAGAA AAAAAAAACA TGCACACACA CACACACACA CACACACACA 60
CACACACACA CACACACACA CATATATATA TATATATATT TTGGTTTTTT TTTTTTTGAG 120
ACGGAGTCTT GCTCTGTCAC CCAGGCTGGA GTGCAGTGGT GTGATCTTGG CTCACTACAA 180
CCTCCACCTC CTGGGTTCAA GCGATTCTCC TGCCTCAGCC TTCTGAGTAG GTGGGATTAC 240
AGGCATGTGC CACCAAGCCT GGCTAATTTT TGTATTTTTA GTAGAGACAG GGTTTCACCA 300
TGTTGGCCAG GCTGGTTAAA AAAATATTTA ACAGGCCGGG TGGTGTGGCT CACGCCTGTA 360
ATCCCAGCAC TTTAGGAGGC CAAAGCAGGC ATATCACCTG AGGTCAGGAG TTTGAGACCA 420
GCCTGAACAA CATGGTGAAA CCCCGTCTCT ACTAAAATTA CAAAAATTAG CCGGGCATGG 480
TGGTGCGCAC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC GTTTGAACCG 540
GGCAGGTGGA GGTTGCAGTG AGCCGAGAGC GTGCCCCTGC CCTCCAGCCT GGGTGACAGC 600
GAGACTTGGT CTCAAAAAAA TAAAAAAAAT AATAAAAAAA GGACCTACCT TACACAATTG 660
TGGATAAAAT GAAGTAATGC ATGAAAGCGG TTAGCACAGA GCCTGGCACA TAGTAAACAC 720
TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT CAGTTCGATA 780
CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG 840
CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG 900
GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC 960
CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG 1020
CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT 1080
CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG 1140
CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG 1200
CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC 1260
CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC 1320
GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT 1380
GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC 1440
CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG 1500
TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA 1560
GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA 1620
CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA 1680
CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG 1740
GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC 1800
AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT 1860
TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA 1920
AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC 1980
GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG 2040
ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT 2100
CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC 2160
TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC 2220
CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG 2280
GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG 2340
GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC 2400
ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG 2460
GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG 2520
AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC 2580
TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC 2640
TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG 2700
AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC 2750
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