EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-00916 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr1:33218780-33222070 
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
GCTGGTTAAA AAAATATTTA ACAGGCCGGG TGGTGTGGCT CACGCCTGTA ATCCCAGCAC 60
TTTAGGAGGC CAAAGCAGGC ATATCACCTG AGGTCAGGAG TTTGAGACCA GCCTGAACAA 120
CATGGTGAAA CCCCGTCTCT ACTAAAATTA CAAAAATTAG CCGGGCATGG TGGTGCGCAC 180
CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC GTTTGAACCG GGCAGGTGGA 240
GGTTGCAGTG AGCCGAGAGC GTGCCCCTGC CCTCCAGCCT GGGTGACAGC GAGACTTGGT 300
CTCAAAAAAA TAAAAAAAAT AATAAAAAAA GGACCTACCT TACACAATTG TGGATAAAAT 360
GAAGTAATGC ATGAAAGCGG TTAGCACAGA GCCTGGCACA TAGTAAACAC TAAGTAAAAG 420
GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT CAGTTCGATA CATTTGTACA 480
CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG 540
GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG 600
TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG 660
GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG CGCGCCAGGC 720
CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT CGGGGGCGTG 780
GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC 840
GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC 900
CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG 960
CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG 1020
CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT GCCCCCTCCC 1080
GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC CCACCCCTCA 1140
CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG TACATGTTCG 1200
CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA GACACAGGAT 1260
CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA CAGCCTGAGA 1320
CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA CACCCACGCG 1380
CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG GTACAGTTGC 1440
CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC AACCGGACTC 1500
GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT TCCCAGATCT 1560
TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA AAGGTGGAAG 1620
GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC GCGATCGGGA 1680
GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG ACTTCTCCCC 1740
GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT CCCCCTTTCA 1800
ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC TCCGCGGGTC 1860
ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC CCAAGAGATG 1920
GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG 1980
AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG GGCAGGGTGA 2040
TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA 2100
TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC 2160
TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG AGATTCCGAA 2220
CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA 2280
AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC TTGAGCAGAT 2340
TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG AAATCAGGGG 2400
CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC CATTTCATGG ATGACGAGAC 2460
TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC TGTGGTGGTT TGAGGTAGTA 2520
ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT CAGTTAGGCT CTTTGAGGAT 2580
TTCTCAGAAG GTAGGTGTTG ATGAGAATCT CCAGGACCTT CCAGCACTCT CCCTGCCCCA 2640
GCAGTCCTGA AAGCCCTGTC TGTGCCTACC TGTCTCTCCT AGAATCTGCA CTAAGGGGGC 2700
AGGGCTGGGG CTCTTCATCT GTCCTCTGAT GGTCGCTCGG ATCTGATGGT TTCCTAGGAA 2760
CTAACTGTGG GCCCAGACTT GTGACCATTT GTGATGGAGG AGAGAGAAGA TAAGAAGGCT 2820
GTGTTTATAG TCTCTTGCCT ACTGGCCCTT GAGGAAGTGG CCTGGGGCTT CCAGCAACAC 2880
TTGTGAGCTT CCAGTTCCTG CTGCAACTTA TGGGTCAACT CAAGCTTTAA GGCGTTCTGA 2940
AAAAAATTAG AAAGCAATGT CAAGACAACA CAGAAATTAA GTGTGAGGGG CTAGGAAATA 3000
TTCTAGGCAA TATATCAAAA GCCTTCTGGG TTGGGGTCAG CTTTAGAAAA CTGAGGAGAT 3060
GGTCCTAATT TGTCTTTGAA GTAATCACAG GATTGAAATT AGTCCTAAAT TGTTGGTTAA 3120
ATGAGAGAAC CAGGGATTTG TTTCAGCTGT GGGGTATGGC CGTGAGTAAA GGCATGGAGT 3180
TGAGGTCAGG CGAGGTGGTT TATGCCTGTA ATCCCAGCAT TTTGGGAGGC CGAGATGGGA 3240
GGATAACTTG AGCCCAGGAG TTTGAGAGTA GCTTGGGGCA ACATGACGAG 3290