| Tag | Content |
|---|
EnhancerAtlas ID | HS098-01329 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:33219140-33221370 |
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 | GAAGTAATGC ATGAAAGCGG TTAGCACAGA GCCTGGCACA TAGTAAACAC TAAGTAAAAG 60
GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT CAGTTCGATA CATTTGTACA 120
CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG 180
GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG 240
TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG 300
GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC 360
CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG 420
GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC 480
GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC 540
CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG 600
CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG 660
CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC 720
GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA 780
CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG 840
CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT 900
CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA 960
CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG 1020
CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC 1080
CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC 1140
GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT 1200
TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG 1260
GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA 1320
GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC 1380
GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA 1440
ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC 1500
ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG 1560
GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG 1620
AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA 1680
TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA 1740
TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC 1800
TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA 1860
CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA 1920
AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT 1980
TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG AAATCAGGGG 2040
CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC CATTTCATGG ATGACGAGAC 2100
TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC TGTGGTGGTT TGAGGTAGTA 2160
ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT CAGTTAGGCT CTTTGAGGAT 2220
TTCTCAGAAG 2230
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