| Tag | Content |
|---|
EnhancerAtlas ID | HS024-00496 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:33218980-33221820 |
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: 3 | Chromosome | Start | End |
| chr1 | 33221184 | 33221695 | | chr1 | 33219489 | 33220800 | | chr1 | 33220987 | 33221800 |
|
Enhancer Sequence | GAGGCTGAGG CAGGAGAATC GTTTGAACCG GGCAGGTGGA GGTTGCAGTG AGCCGAGAGC 60
GTGCCCCTGC CCTCCAGCCT GGGTGACAGC GAGACTTGGT CTCAAAAAAA TAAAAAAAAT 120
AATAAAAAAA GGACCTACCT TACACAATTG TGGATAAAAT GAAGTAATGC ATGAAAGCGG 180
TTAGCACAGA GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC 240
TGTAACTACA GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC 300
GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC 360
CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA 420
CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA 480
GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC 540
GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC 600
GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC 660
CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT 720
CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC 780
GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG 840
GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT 900
GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG 960
TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC 1020
ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA 1080
CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA 1140
TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA 1200
CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG 1260
ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA 1320
CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG 1380
GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG 1440
GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC 1500
TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC 1560
CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA 1620
CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG 1680
GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC 1740
AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT 1800
AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC 1860
CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG 1920
TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG 1980
GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT 2040
CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC 2100
AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC 2160
ACTCTGGCTC CTACAGGGGT TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA 2220
CACTTACTGT TCTGGCTAGC CATTTCATGG ATGACGAGAC TGAGGTCCAG GAAAGAGGGA 2280
CTTGTCCAAG GTCATTTGCC TGTGGTGGTT TGAGGTAGTA ATATAATCAA AATGACAATA 2340
AGAAAAGGGT TAACTAAGTT CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG 2400
ATGAGAATCT CCAGGACCTT CCAGCACTCT CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC 2460
TGTGCCTACC TGTCTCTCCT AGAATCTGCA CTAAGGGGGC AGGGCTGGGG CTCTTCATCT 2520
GTCCTCTGAT GGTCGCTCGG ATCTGATGGT TTCCTAGGAA CTAACTGTGG GCCCAGACTT 2580
GTGACCATTT GTGATGGAGG AGAGAGAAGA TAAGAAGGCT GTGTTTATAG TCTCTTGCCT 2640
ACTGGCCCTT GAGGAAGTGG CCTGGGGCTT CCAGCAACAC TTGTGAGCTT CCAGTTCCTG 2700
CTGCAACTTA TGGGTCAACT CAAGCTTTAA GGCGTTCTGA AAAAAATTAG AAAGCAATGT 2760
CAAGACAACA CAGAAATTAA GTGTGAGGGG CTAGGAAATA TTCTAGGCAA TATATCAAAA 2820
GCCTTCTGGG TTGGGGTCAG 2840
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