| Tag | Content |
|---|
EnhancerAtlas ID | HS105-01999 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:33219100-33221690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:33221585-33221596 | GAAGATAAGAA | - | 6.02 | | 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 | | ZNF263 | MA0528.1 | chr1:33221575-33221596 | GGAGGAGAGAGAAGATAAGAA | + | 6.32 |
|
| | Number of super-enhancer constituents: 24 | 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_23802 | chr1:33221322-33221788 | 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 | AATAAAAAAA GGACCTACCT TACACAATTG TGGATAAAAT GAAGTAATGC ATGAAAGCGG 60
TTAGCACAGA GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC 120
TGTAACTACA GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC 180
GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC 240
CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA 300
CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA 360
GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC 420
GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC 480
GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC 540
CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT 600
CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC 660
GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG 720
GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT 780
GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG 840
TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC 900
ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA 960
CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA 1020
TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA 1080
CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG 1140
ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA 1200
CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG 1260
GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG 1320
GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC 1380
TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC 1440
CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA 1500
CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG 1560
GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC 1620
AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT 1680
AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC 1740
CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG 1800
TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG 1860
GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT 1920
CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC 1980
AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC 2040
ACTCTGGCTC CTACAGGGGT TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA 2100
CACTTACTGT TCTGGCTAGC CATTTCATGG ATGACGAGAC TGAGGTCCAG GAAAGAGGGA 2160
CTTGTCCAAG GTCATTTGCC TGTGGTGGTT TGAGGTAGTA ATATAATCAA AATGACAATA 2220
AGAAAAGGGT TAACTAAGTT CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG 2280
ATGAGAATCT CCAGGACCTT CCAGCACTCT CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC 2340
TGTGCCTACC TGTCTCTCCT AGAATCTGCA CTAAGGGGGC AGGGCTGGGG CTCTTCATCT 2400
GTCCTCTGAT GGTCGCTCGG ATCTGATGGT TTCCTAGGAA CTAACTGTGG GCCCAGACTT 2460
GTGACCATTT GTGATGGAGG AGAGAGAAGA TAAGAAGGCT GTGTTTATAG TCTCTTGCCT 2520
ACTGGCCCTT GAGGAAGTGG CCTGGGGCTT CCAGCAACAC TTGTGAGCTT CCAGTTCCTG 2580
CTGCAACTTA 2590
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