EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS196-00625 
Organism
Homo sapiens 
Tissue/cell
ZR75-1 
Coordinate
chr1:33218760-33222070 
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
GGTTTCACCA TGTTGGCCAG GCTGGTTAAA AAAATATTTA ACAGGCCGGG TGGTGTGGCT 60
CACGCCTGTA ATCCCAGCAC TTTAGGAGGC CAAAGCAGGC ATATCACCTG AGGTCAGGAG 120
TTTGAGACCA GCCTGAACAA CATGGTGAAA CCCCGTCTCT ACTAAAATTA CAAAAATTAG 180
CCGGGCATGG TGGTGCGCAC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC 240
GTTTGAACCG GGCAGGTGGA GGTTGCAGTG AGCCGAGAGC GTGCCCCTGC CCTCCAGCCT 300
GGGTGACAGC GAGACTTGGT CTCAAAAAAA TAAAAAAAAT AATAAAAAAA GGACCTACCT 360
TACACAATTG TGGATAAAAT GAAGTAATGC ATGAAAGCGG TTAGCACAGA GCCTGGCACA 420
TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT 480
CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT 540
CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG 600
TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC 660
CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC 720
CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG 780
CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG 840
AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT 900
TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC 960
CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA 1020
GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC 1080
CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC 1140
CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG 1200
CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA 1260
CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT 1320
AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC 1380
ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC 1440
GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA 1500
CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA 1560
CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG 1620
AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC 1680
TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG 1740
CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC 1800
CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT 1860
GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG 1920
GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA 1980
TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG 2040
ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC 2100
ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG 2160
TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC 2220
ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT 2280
GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC 2340
CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT 2400
TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC 2460
CATTTCATGG ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC 2520
TGTGGTGGTT TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT 2580
CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT CCAGGACCTT 2640
CCAGCACTCT CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC TGTCTCTCCT 2700
AGAATCTGCA CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT GGTCGCTCGG 2760
ATCTGATGGT TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT GTGATGGAGG 2820
AGAGAGAAGA TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT GAGGAAGTGG 2880
CCTGGGGCTT CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA TGGGTCAACT 2940
CAAGCTTTAA GGCGTTCTGA AAAAAATTAG AAAGCAATGT CAAGACAACA CAGAAATTAA 3000
GTGTGAGGGG CTAGGAAATA TTCTAGGCAA TATATCAAAA GCCTTCTGGG TTGGGGTCAG 3060
CTTTAGAAAA CTGAGGAGAT GGTCCTAATT TGTCTTTGAA GTAATCACAG GATTGAAATT 3120
AGTCCTAAAT TGTTGGTTAA ATGAGAGAAC CAGGGATTTG TTTCAGCTGT GGGGTATGGC 3180
CGTGAGTAAA GGCATGGAGT TGAGGTCAGG CGAGGTGGTT TATGCCTGTA ATCCCAGCAT 3240
TTTGGGAGGC CGAGATGGGA GGATAACTTG AGCCCAGGAG TTTGAGAGTA GCTTGGGGCA 3300
ACATGACGAG 3310