EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-00294 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr1:16501810-16504160 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr1:16503374-16503391TGCTTCCTAGGAAGTGA+6.08
RREB1MA0073.1chr1:16502026-16502046TGTGAGGGGGTGGGAGGGGG-6.61
RREB1MA0073.1chr1:16502036-16502056TGGGAGGGGGTGGGATGGGG-7.16
SOX10MA0442.2chr1:16502839-16502850TTCTTTGTTTT-6.62
ZNF263MA0528.1chr1:16503057-16503078CATCCTCCTCCATCCTCCTCC-6.3
ZNF263MA0528.1chr1:16503060-16503081CCTCCTCCATCCTCCTCCTCC-8.07
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_23091chr1:16501962-16502745Colon_Crypt_1
SE_23091chr1:16502844-16503560Colon_Crypt_1
SE_23091chr1:16503896-16504683Colon_Crypt_1
SE_23751chr1:16502050-16502674Colon_Crypt_2
SE_23751chr1:16502855-16503434Colon_Crypt_2
SE_24743chr1:16497841-16502803Colon_Crypt_3
SE_24743chr1:16502816-16503501Colon_Crypt_3
SE_26540chr1:16496436-16504779Esophagus
SE_28102chr1:16497879-16504574Fetal_Intestine
SE_29455chr1:16497964-16506131Fetal_Intestine_Large
SE_31527chr1:16499336-16504399Gastric
SE_34268chr1:16497740-16504248HCT-116
SE_34628chr1:16497415-16506115HeLa
SE_36144chr1:16502024-16503485HMEC
SE_38062chr1:16499064-16503878HUVEC
SE_40833chr1:16501759-16503971Left_Ventricle
SE_44998chr1:16502053-16503662NHLF
SE_46140chr1:16501795-16503844Osteoblasts
SE_47009chr1:16502010-16502676Ovary
SE_47009chr1:16502860-16503560Ovary
SE_47009chr1:16503623-16504003Ovary
SE_47150chr1:16499250-16512083Panc1
SE_47539chr1:16501964-16502662Pancreas
SE_47539chr1:16502819-16503601Pancreas
SE_48744chr1:16501448-16503785Right_Atrium
SE_50427chr1:16497958-16504232Sigmoid_Colon
SE_52536chr1:16501918-16504326Small_Intestine
SE_56795chr1:16499345-16504738VACO_400
SE_57357chr1:16501943-16502709VACO_503
SE_57939chr1:16501961-16502682VACO_9m
SE_57939chr1:16502843-16503425VACO_9m
SE_64726chr1:16502266-16503212NHEK
SE_65472chr1:16501980-16503977Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11650207416503312
Number: 1             
IDChromosomeStartEnd
GH01I016171chr11649794116511884
Enhancer Sequence
TTTTAAGCCC TCGGAGCCTC AGTTTCATGA TCTGTAAAGT GGACATTAGA GTCGCTCGGG 60
ATGCGGGATG CTTGAATGAG ATGATGCACT CAGCACGCGG CAGGCCCTGG GGCCCTGTGT 120
GCTCTACAAT TGCAGCTGCT ATTAGACCAG CTTCTTTCTT GCCTGGGTAT GTGGGGCTTA 180
GGCCAGAACA AATCTTGGGA CTGAGTGTAA AATATATGTG AGGGGGTGGG AGGGGGTGGG 240
ATGGGGCTCG GTGCGGGCCT GGCAGGTGTG CTGGGAGGCA AGGCCTATGA CTCCTGTGGG 300
CCTGCTCTTC CTCCCATCCC ACCCTCCACA GTCCCCACCT CAGGGGCCCT GGGCCTGGGG 360
CAGCAGGGGC CGGGATGTGT CTCTCCAGAG CAGGAACGGA GGGGCCTCCG CAACTGGTTG 420
GGGAGGGGGG GTGGATGCCA GCCCCCGCTG ATTAGGTCTC AAATTAAAGC CGAGCTTGCT 480
CCTGTCGCTG CTCAGGCAGG CCCTCCTCCT GGCCACAGTT CCCTGCCTGG CCCTCTGCTT 540
CGGGCCTCAT GGTGGCTGGT TGCTCCCAGC CTAGAATTGC TAAAAGGCTC CCGTAGTGGG 600
TAGGAGCCTC AGGGGACCTG GGAGAGGCTT CAGGGGCCCT GCCTGTGCGG GGGTCTCTCC 660
TGTGACCCTC AGACCTGAGC CAGTGTCTGG GGACAAGTCA CCGTGTCAGA GGCTGCGGAG 720
AGCAAAGCCC AGGCGGTGAT GACTTGAGTT TCCAGGCCGG GTGCCAGGAG GCCCGCGGTC 780
ACACTCCGCC TGGGGCCTGG GCTCCGGCCA ACTGTCAGCA GCAGAGATTG TTGGGTTGGT 840
TTTATTTTAA ACAAAAAAGA ACTTTGAGTG GAAACATGTG TTTCTTTTTT CTCCCCCTTC 900
CCTCTCTCCC TATCTCTCTC CATCTCATCA TGGAATATTT CTCTTTTTTG TACCTCCCTT 960
TCTCTGTTTT TCTCTCTGTC TTCCTCTATT TGTCCCTGCC TCTGTCTCTC TCTCTCTCTC 1020
TCTCATTCTT TCTTTGTTTT CCTATCTCTT GATTTCTCTG TCTCTTTCTC TATTTCTTTT 1080
TCCGCAGCTT TCAGGAGTCA GGAGAGGTAC CAGACTTCCT CCCTCGGGGT GTGGCCTGGG 1140
CCCCTGCCAT AAAATCCCCA GGCGTGCCAC GGCCCTATGT CGGGGGTCTG CCGCTCCAGG 1200
GGAGGGAGGG GGTGTCTAGC AGCGGAGGCT CCAGGACCCA AATGCTCCAT CCTCCTCCAT 1260
CCTCCTCCTC CAAGCTCCCA CTGCCCCTGC ATCTGCCCTT CCTGTGTCTG TTTTCTCTAC 1320
TAAGCATCTA GAAAATAATT CTGCAGCTTG AGACAAGTTT TAAAACACTG GTCTGGCCCA 1380
AACCACCCAT CTACAGCCAG AGACTGGCGC CGAGGAGGGG ACCATGGCCT GCTCAACACC 1440
GCACGGAGGG TTAGGGGCAA AGCCAGGCCG ACCCAGGTCC CCCACTCCCA AGTGACATTA 1500
CTGACACCCC CAAACCCACA GTCACCACAC TTCTCAGGTC CCTGCGTCTT TCAGAGGGGT 1560
GGTCTGCTTC CTAGGAAGTG ATGTGCCCTC CCCTAAGGTG GTCACCCAGC ACAAGGGTCC 1620
CCCTGGAAAA TGTCCTGCCT TGGCTGGTCA CCCCTCCCCC AGGACAGACA AGCTTTTGGG 1680
CCCCCACCTT TCAGCCCCTT CTGCCAGGCA GTAGAGAAGA GAGAAGAGAG ACTCGCAGGC 1740
ACAGTGGCTC ATGCCTGTAA TCCTAGCACT TTGGGAGGCC GAGGTGGGCA GATCACAAGG 1800
TCAGGAGATA CAGAAGAGAG ACTGGCCACC CATGCACTGG GCCCAGGTCC TAGCTCGACG 1860
TCTGAGTCCT TGTGTGACTG TGAATATGAC TTTTCCACTG GCTGGCCTCA GTTTCCCCAT 1920
CTTTGTAACA GAAGCCTTGC CTTTGCCGCG GATCCCCTCT CTGCTCTAAT ATGTTATGGT 1980
GTTCTCCTCT CCTTCCATGG AGAGGAATTC TGGAACATCA GACCAGGAGT GCCATCTCCT 2040
CTCCCAAAGT GAGAGGGACT GTCCTCAGTG TGGCCTCAAT AGGTCAACTC CCCTTCACTT 2100
CAGGTTCCTT GTCCCCTGTG TGCAAGGGCC CCAGATGCCA CCACCAAGGG GAGAGGTGCC 2160
ACCATGACCT GGTGCACCAT TGTCAAAGGT GCACTTTCTT GGGTGTCCGG GGTCATGCCA 2220
GGATTCATGC AGGGATAGGA GGGGCTGCCT GCGTGTCAGG GGCCCATTCC ACCCCTGTCT 2280
CCCACAGCCC CAGGAGTAAA GTCAGGGTAA GTGTGCGGGA TTAGTAAGGT GGGGACACGG 2340
GAGACTGTCT 2350