EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS158-01388 
Organism
Homo sapiens 
Tissue/cell
Pancreas 
Coordinate
chr1:33218910-33221720 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr1:33221585-33221596GAAGATAAGAA-6.02
KLF16MA0741.1chr1:33219795-33219806GGGGGCGGGGC-6.02
KLF16MA0741.1chr1:33219551-33219562GGGGGCGTGGT-6.14
KLF5MA0599.1chr1:33219498-33219508GCCCCGCCCC+6.02
KLF5MA0599.1chr1:33219796-33219806GGGGCGGGGC-6.02
SP1MA0079.4chr1:33219495-33219510CAGGCCCCGCCCCTC+6.22
SP4MA0685.1chr1:33219495-33219512CAGGCCCCGCCCCTCCT+6.32
ZNF263MA0528.1chr1:33220523-33220544TCCCCCCCTCCCCCGTCCCCA-6.03
ZNF263MA0528.1chr1:33220656-33220677TGGGGAGGGGAGGGAAAGGGG+6.2
ZNF263MA0528.1chr1:33221575-33221596GGAGGAGAGAGAAGATAAGAA+6.32
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_00938chr1:33219006-33222393Adrenal_Gland
SE_23116chr1:33219622-33222368Colon_Crypt_1
SE_23802chr1:33219124-33219553Colon_Crypt_2
SE_23802chr1:33219604-33220504Colon_Crypt_2
SE_23802chr1:33220519-33221309Colon_Crypt_2
SE_23802chr1:33221322-33221788Colon_Crypt_2
SE_24863chr1:33219103-33221902Colon_Crypt_3
SE_26629chr1:33219003-33222323Esophagus
SE_28121chr1:33220540-33221955Fetal_Intestine
SE_29204chr1:33219822-33221616Fetal_Intestine_Large
SE_31442chr1:33219069-33222394Gastric
SE_32998chr1:33219539-33221354H1
SE_34017chr1:33218987-33219471HCC1954
SE_34017chr1:33219830-33221722HCC1954
SE_36587chr1:33219820-33221157HMEC
SE_41588chr1:33219113-33221709LNCaP
SE_47530chr1:33219105-33219467Pancreas
SE_47530chr1:33219506-33221824Pancreas
SE_50335chr1:33220528-33222187Sigmoid_Colon
SE_52480chr1:33219537-33222050Small_Intestine
SE_64801chr1:33219051-33219585NHEK
SE_64801chr1:33219594-33221668NHEK
SE_65538chr1:33218762-33221927Pancreatic_islets
SE_68878chr1:33219160-33221410H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr13322118433221695
chr13321948933220800
Enhancer Sequence
CCCCGTCTCT ACTAAAATTA CAAAAATTAG CCGGGCATGG TGGTGCGCAC CTGTAGTCCC 60
AGCTACTCGG GAGGCTGAGG CAGGAGAATC GTTTGAACCG GGCAGGTGGA GGTTGCAGTG 120
AGCCGAGAGC GTGCCCCTGC CCTCCAGCCT GGGTGACAGC GAGACTTGGT CTCAAAAAAA 180
TAAAAAAAAT AATAAAAAAA GGACCTACCT TACACAATTG TGGATAAAAT GAAGTAATGC 240
ATGAAAGCGG TTAGCACAGA GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA 300
TTTTGAACAC TGTAACTACA GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG 360
TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT 420
CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC 480
GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC 540
CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC 600
CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG 660
GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG 720
GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA 780
ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG 840
CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC 900
AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA 960
GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG 1020
GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC 1080
AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC 1140
ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA 1200
TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA 1260
CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT 1320
AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC 1380
TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA 1440
CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG 1500
GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG 1560
TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC 1620
CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC 1680
CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG 1740
CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT 1800
TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC 1860
GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT 1920
CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG 1980
TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA 2040
GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG 2100
ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC 2160
CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT 2220
TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG AAATCAGGGG CCCTAGGTGA 2280
CTTCTTGGGA CACTTACTGT TCTGGCTAGC CATTTCATGG ATGACGAGAC TGAGGTCCAG 2340
GAAAGAGGGA CTTGTCCAAG GTCATTTGCC TGTGGTGGTT TGAGGTAGTA ATATAATCAA 2400
AATGACAATA AGAAAAGGGT TAACTAAGTT CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG 2460
GTAGGTGTTG ATGAGAATCT CCAGGACCTT CCAGCACTCT CCCTGCCCCA GCAGTCCTGA 2520
AAGCCCTGTC TGTGCCTACC TGTCTCTCCT AGAATCTGCA CTAAGGGGGC AGGGCTGGGG 2580
CTCTTCATCT GTCCTCTGAT GGTCGCTCGG ATCTGATGGT TTCCTAGGAA CTAACTGTGG 2640
GCCCAGACTT GTGACCATTT GTGATGGAGG AGAGAGAAGA TAAGAAGGCT GTGTTTATAG 2700
TCTCTTGCCT ACTGGCCCTT GAGGAAGTGG CCTGGGGCTT CCAGCAACAC TTGTGAGCTT 2760
CCAGTTCCTG CTGCAACTTA TGGGTCAACT CAAGCTTTAA GGCGTTCTGA 2810