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

TagContent
EnhancerAtlas ID
HS034-00843 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr1:33219070-33221700 
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
GAGACTTGGT CTCAAAAAAA TAAAAAAAAT AATAAAAAAA GGACCTACCT TACACAATTG 60
TGGATAAAAT GAAGTAATGC ATGAAAGCGG TTAGCACAGA GCCTGGCACA TAGTAAACAC 120
TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT CAGTTCGATA 180
CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG 240
CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG 300
GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC 360
CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG 420
CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT 480
CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG 540
CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG 600
CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC 660
CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC 720
GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT 780
GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC 840
CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG 900
TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA 960
GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA 1020
CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA 1080
CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG 1140
GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC 1200
AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT 1260
TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA 1320
AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC 1380
GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG 1440
ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT 1500
CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC 1560
TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC 1620
CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG 1680
GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG 1740
GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC 1800
ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG 1860
GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG 1920
AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC 1980
TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC 2040
TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG 2100
AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC CATTTCATGG 2160
ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC TGTGGTGGTT 2220
TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT CAGTTAGGCT 2280
CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT CCAGGACCTT CCAGCACTCT 2340
CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC TGTCTCTCCT AGAATCTGCA 2400
CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT GGTCGCTCGG ATCTGATGGT 2460
TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT GTGATGGAGG AGAGAGAAGA 2520
TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT GAGGAAGTGG CCTGGGGCTT 2580
CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA TGGGTCAACT 2630