| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01205 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:33219180-33221930 |
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 | TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT 60
CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT 120
CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG 180
TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC 240
CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC 300
CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG 360
CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG 420
AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT 480
TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC 540
CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA 600
GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC 660
CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC 720
CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG 780
CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA 840
CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT 900
AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC 960
ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC 1020
GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA 1080
CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA 1140
CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG 1200
AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC 1260
TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG 1320
CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC 1380
CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT 1440
GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG 1500
GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA 1560
TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG 1620
ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC 1680
ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG 1740
TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC 1800
ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT 1860
GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC 1920
CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT 1980
TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC 2040
CATTTCATGG ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC 2100
TGTGGTGGTT TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT 2160
CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT CCAGGACCTT 2220
CCAGCACTCT CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC TGTCTCTCCT 2280
AGAATCTGCA CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT GGTCGCTCGG 2340
ATCTGATGGT TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT GTGATGGAGG 2400
AGAGAGAAGA TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT GAGGAAGTGG 2460
CCTGGGGCTT CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA TGGGTCAACT 2520
CAAGCTTTAA GGCGTTCTGA AAAAAATTAG AAAGCAATGT CAAGACAACA CAGAAATTAA 2580
GTGTGAGGGG CTAGGAAATA TTCTAGGCAA TATATCAAAA GCCTTCTGGG TTGGGGTCAG 2640
CTTTAGAAAA CTGAGGAGAT GGTCCTAATT TGTCTTTGAA GTAATCACAG GATTGAAATT 2700
AGTCCTAAAT TGTTGGTTAA ATGAGAGAAC CAGGGATTTG TTTCAGCTGT 2750
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