| Tag | Content |
|---|
EnhancerAtlas ID | HS129-00806 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:33219310-33221890 |
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: 21 | ID | Coordinate | Tissue/cell |
| SE_00938 | chr1:33219006-33222393 | Adrenal_Gland | | SE_23116 | chr1:33219622-33222368 | Colon_Crypt_1 | | 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 | chr1:33219830-33221722 | HCC1954 | | SE_36587 | chr1:33219820-33221157 | HMEC | | SE_41588 | chr1:33219113-33221709 | LNCaP | | 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 | CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG 60
GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC 120
CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG 180
CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT 240
CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG 300
CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG 360
CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC 420
CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC 480
GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT 540
GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC 600
CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG 660
TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA 720
GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA 780
CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA 840
CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG 900
GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC 960
AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT 1020
TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA 1080
AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC 1140
GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG 1200
ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT 1260
CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC 1320
TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC 1380
CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG 1440
GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG 1500
GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC 1560
ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG 1620
GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG 1680
AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC 1740
TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC 1800
TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG 1860
AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC CATTTCATGG 1920
ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC TGTGGTGGTT 1980
TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT CAGTTAGGCT 2040
CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT CCAGGACCTT CCAGCACTCT 2100
CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC TGTCTCTCCT AGAATCTGCA 2160
CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT GGTCGCTCGG ATCTGATGGT 2220
TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT GTGATGGAGG AGAGAGAAGA 2280
TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT GAGGAAGTGG CCTGGGGCTT 2340
CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA TGGGTCAACT CAAGCTTTAA 2400
GGCGTTCTGA AAAAAATTAG AAAGCAATGT CAAGACAACA CAGAAATTAA GTGTGAGGGG 2460
CTAGGAAATA TTCTAGGCAA TATATCAAAA GCCTTCTGGG TTGGGGTCAG CTTTAGAAAA 2520
CTGAGGAGAT GGTCCTAATT TGTCTTTGAA GTAATCACAG GATTGAAATT AGTCCTAAAT 2580
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