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

TagContent
EnhancerAtlas ID
HS134-00841 
Organism
Homo sapiens 
Tissue/cell
Mesendoderm 
Coordinate
chr1:33219170-33222040 
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: 3             
ChromosomeStartEnd
chr13322118433221695
chr13321948933220800
chr13322098733221800
Enhancer Sequence
GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA 60
GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG 120
CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC 180
CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG 240
CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA 300
GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC 360
TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG 420
CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT 480
GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA 540
GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA 600
GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG 660
CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT 720
CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA 780
TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA 840
CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA 900
CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT 960
TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT 1020
CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC 1080
AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA 1140
CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT 1200
TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT 1260
GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA 1320
CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC 1380
CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT 1440
GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG 1500
AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA 1560
GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT 1620
GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG 1680
GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC 1740
CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC 1800
AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG 1860
AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG 1920
TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC 1980
CTACAGGGGT TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT 2040
TCTGGCTAGC CATTTCATGG ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG 2100
GTCATTTGCC TGTGGTGGTT TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT 2160
TAACTAAGTT CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT 2220
CCAGGACCTT CCAGCACTCT CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC 2280
TGTCTCTCCT AGAATCTGCA CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT 2340
GGTCGCTCGG ATCTGATGGT TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT 2400
GTGATGGAGG AGAGAGAAGA TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT 2460
GAGGAAGTGG CCTGGGGCTT CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA 2520
TGGGTCAACT CAAGCTTTAA GGCGTTCTGA AAAAAATTAG AAAGCAATGT CAAGACAACA 2580
CAGAAATTAA GTGTGAGGGG CTAGGAAATA TTCTAGGCAA TATATCAAAA GCCTTCTGGG 2640
TTGGGGTCAG CTTTAGAAAA CTGAGGAGAT GGTCCTAATT TGTCTTTGAA GTAATCACAG 2700
GATTGAAATT AGTCCTAAAT TGTTGGTTAA ATGAGAGAAC CAGGGATTTG TTTCAGCTGT 2760
GGGGTATGGC CGTGAGTAAA GGCATGGAGT TGAGGTCAGG CGAGGTGGTT TATGCCTGTA 2820
ATCCCAGCAT TTTGGGAGGC CGAGATGGGA GGATAACTTG AGCCCAGGAG 2870