EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS167-01212 
Organism
Homo sapiens 
Tissue/cell
Retina 
Coordinate
chr1:33218630-33221700 
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
GTGATCTTGG CTCACTACAA CCTCCACCTC CTGGGTTCAA GCGATTCTCC TGCCTCAGCC 60
TTCTGAGTAG GTGGGATTAC AGGCATGTGC CACCAAGCCT GGCTAATTTT TGTATTTTTA 120
GTAGAGACAG GGTTTCACCA TGTTGGCCAG GCTGGTTAAA AAAATATTTA ACAGGCCGGG 180
TGGTGTGGCT CACGCCTGTA ATCCCAGCAC TTTAGGAGGC CAAAGCAGGC ATATCACCTG 240
AGGTCAGGAG TTTGAGACCA GCCTGAACAA CATGGTGAAA CCCCGTCTCT ACTAAAATTA 300
CAAAAATTAG CCGGGCATGG TGGTGCGCAC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG 360
CAGGAGAATC GTTTGAACCG GGCAGGTGGA GGTTGCAGTG AGCCGAGAGC GTGCCCCTGC 420
CCTCCAGCCT GGGTGACAGC GAGACTTGGT CTCAAAAAAA TAAAAAAAAT AATAAAAAAA 480
GGACCTACCT TACACAATTG TGGATAAAAT GAAGTAATGC ATGAAAGCGG TTAGCACAGA 540
GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA 600
GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG 660
CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC 720
CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG 780
CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA 840
GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC 900
TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG 960
CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT 1020
GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA 1080
GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA 1140
GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG 1200
CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT 1260
CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA 1320
TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA 1380
CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA 1440
CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT 1500
TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT 1560
CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC 1620
AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA 1680
CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT 1740
TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT 1800
GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA 1860
CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC 1920
CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT 1980
GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG 2040
AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA 2100
GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT 2160
GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG 2220
GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC 2280
CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC 2340
AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG 2400
AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG 2460
TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC 2520
CTACAGGGGT TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT 2580
TCTGGCTAGC CATTTCATGG ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG 2640
GTCATTTGCC TGTGGTGGTT TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT 2700
TAACTAAGTT CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT 2760
CCAGGACCTT CCAGCACTCT CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC 2820
TGTCTCTCCT AGAATCTGCA CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT 2880
GGTCGCTCGG ATCTGATGGT TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT 2940
GTGATGGAGG AGAGAGAAGA TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT 3000
GAGGAAGTGG CCTGGGGCTT CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA 3060
TGGGTCAACT 3070