EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS161-01653 
Organism
Homo sapiens 
Tissue/cell
PC3 
Coordinate
chr1:235090320-235093080 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs908327chr1235092600hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr1:235091354-235091369AGGGGGCAGAGGGCA+6.63
Nr2f6(var.2)MA0728.1chr1:235092071-235092086GAGGTCATGAGTTCA+6.26
RARAMA0729.1chr1:235092071-235092089GAGGTCATGAGTTCAAGA+6.12
Six3MA0631.1chr1:235091720-235091737GCAAATGATACCCTTTC-6.12
TFAP2CMA0524.2chr1:235090469-235090481CGCCCCAGGGCA+6.22
ZNF263MA0528.1chr1:235091129-235091150GGAGCAGCTGGAGGAGGGGAG+6.02
Number of super-enhancer constituents: 70             
IDCoordinateTissue/cell
SE_00182chr1:235089787-235092321Adipose_Nuclei
SE_00983chr1:235090315-235091537Adrenal_Gland
SE_00983chr1:235092569-235093035Adrenal_Gland
SE_01666chr1:235090775-235091665Aorta
SE_01666chr1:235092553-235095108Aorta
SE_02305chr1:235090797-235091817Astrocytes
SE_04136chr1:235089974-235090679Brain_Anterior_Caudate
SE_04136chr1:235091089-235091897Brain_Anterior_Caudate
SE_06052chr1:235092563-235095925Brain_Hippocampus_Middle
SE_07547chr1:235089887-235092129Brain_Hippocampus_Middle_150
SE_09160chr1:235089274-235102029CD14
SE_13412chr1:235090132-235091861CD34_Primary_RO01536
SE_13412chr1:235092302-235095085CD34_Primary_RO01536
SE_14852chr1:235090111-235096258CD4_Memory_Primary_7pool
SE_19577chr1:235090565-235091808CD4p_CD25-_Il17p_PMAstim_Th17
SE_21117chr1:235090472-235092194CD8_Memory_7pool
SE_21117chr1:235092380-235094348CD8_Memory_7pool
SE_23314chr1:235090322-235090800Colon_Crypt_1
SE_23314chr1:235090805-235091803Colon_Crypt_1
SE_23314chr1:235092463-235096122Colon_Crypt_1
SE_23955chr1:235090350-235090759Colon_Crypt_2
SE_23955chr1:235090824-235091497Colon_Crypt_2
SE_23955chr1:235092554-235093067Colon_Crypt_2
SE_25800chr1:235089687-235101859Duodenum_Smooth_Muscle
SE_26806chr1:235090349-235091700Esophagus
SE_26806chr1:235092605-235093136Esophagus
SE_27663chr1:235089063-235101555Fetal_Intestine
SE_28576chr1:235088850-235101396Fetal_Intestine_Large
SE_29689chr1:235090283-235092133Fetal_Muscle
SE_29689chr1:235092238-235094048Fetal_Muscle
SE_31235chr1:235090341-235091774Fetal_Thymus
SE_31235chr1:235092263-235094078Fetal_Thymus
SE_31572chr1:235090061-235091822Gastric
SE_31572chr1:235091850-235096149Gastric
SE_32492chr1:235088942-235092206GM12878
SE_33758chr1:235092170-235101690HCC1954
SE_34767chr1:235092103-235099043HeLa
SE_36952chr1:235089804-235094553HSMMtube
SE_40307chr1:235092364-235094852K562
SE_40653chr1:235089852-235091891Left_Ventricle
SE_41640chr1:235092557-235093028LNCaP
SE_42265chr1:235089721-235091735Lung
SE_43462chr1:235092226-235096141MCF-7
SE_44805chr1:235090559-235091810NHLF
SE_45558chr1:235090190-235094180Osteoblasts
SE_47119chr1:235087515-235103374Panc1
SE_47599chr1:235090912-235091521Pancreas
SE_47599chr1:235092519-235093108Pancreas
SE_48697chr1:235089896-235091719Right_Atrium
SE_50040chr1:235092229-235094403RPMI-8402
SE_50071chr1:235089709-235100691Sigmoid_Colon
SE_51271chr1:235089831-235092066Skeletal_Muscle
SE_51271chr1:235092438-235095754Skeletal_Muscle
SE_51773chr1:235090507-235091828Skeletal_Muscle_Myoblast
SE_51773chr1:235092334-235094038Skeletal_Muscle_Myoblast
SE_52352chr1:235089712-235101497Small_Intestine
SE_53330chr1:235089854-235092349Spleen
SE_54553chr1:235090275-235096009Stomach_Smooth_Muscle
SE_56068chr1:235090847-235091959u87
SE_56760chr1:235090862-235091499VACO_400
SE_56760chr1:235092552-235093115VACO_400
SE_59259chr1:235089283-235124733Ly3
SE_60969chr1:235059965-235155853HBL1
SE_61435chr1:234961094-235124239Toledo
SE_62329chr1:235047040-235185428Tonsil
SE_63542chr1:235090473-235091948HSMM
SE_63542chr1:235092307-235094054HSMM
SE_65393chr1:235090044-235091867Pancreatic_islets
SE_65393chr1:235092372-235101616Pancreatic_islets
SE_67736chr1:235090847-235091959u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1235090546235090894
chr1235091073235091332
chr1235091427235091813
Number: 1             
IDChromosomeStartEnd
GH01I234953chr1235089124235101946
Enhancer Sequence
TGGTGACCTC CTATTTCTTA AATGCTCATA ACTAAATCAA ATTGTTTTAA ATATCATTCC 60
GGCCAAAAAA AACCCCATTT GATGCTCCTG ATGAGGTCCG TGAGGTCCGA GACCCCTGCA 120
TGAACCAGTC AGATCACCAT GGAACAAGTC GCCCCAGGGC ATGGCTGTCT CCAGCCGCTC 180
TGAGTAGCCA GCGGTGCAGC CAGCTGGTCT CAGATTTGGG CTGTGATGAG TCTGGATGGC 240
AGAAGAACAA GAGGGATGGG AAATTGAGGG AGGGCCTCAT TGAAAGGGCT CACTCCAGGA 300
GCCAGAAAAC CAGAAGAGCC TAAGGGACCC AGAGCTAGAG TGAGACCAGA GATGCACAGT 360
CCCCATGAGG ACAAAGAGCC CAGTGAGGAG AAAGGGAGAG GTAAAAGGAT AAAAGAGTCA 420
GAAGGAGTTT CAGAATCTAA GAGCTCCAAA AATAAACCTT TCCCTTTGTA TCACTTTTCT 480
CTTTTTACTT TAGTTGCTCT CAACTTGCTG CTTCCTTTTT TTAAAAATTC TAGCAATTCT 540
GCAGGAAACC AGAAGTGTGA ACCAAACACA GTAACTCTAG GTGTTATGGC GCTGTCCTGC 600
TCACCCTTCT TTTGGCCTAC TGGCTTCAAA GGTAGGCACA CACACCGTCC CTTTTCTAAT 660
GATCCGGTCG TGGATTCAGG CTCAGTAAGC CAAGACCACA AGCAACAGGG CTTGGGCTCC 720
ATCTGCCTCG GCTGCTTGCA GCTGCCTTCC AGGAAGTGCT GGAACAGCAG AAGCAGCTAG 780
CAGTGCGCTC AAGAAGTGGT CAGCAGTTGG GAGCAGCTGG AGGAGGGGAG GCCAGTGAGC 840
AAGTATCAGC TTGGGAAATA GGGTTTCGGC TGAACAAAGT TCACTGCTGT TTTCTGAGAA 900
AGCAGAACCT AGTGGAGCCA CCCTAGAGAA TAAGGAGAGG AGCAACTGGA ACTGAGTGTT 960
GGCTCCAAAC TTCCACGGCA TGATATGCTT GGCCACCCAA TTGTGATCAG GGCCATTGTT 1020
GTTCCCCTGG GGGCAGGGGG CAGAGGGCAG GCCGCCGCTC GGAGTAAAAA GGGAAGACAG 1080
ACAGGCAGTC CAAACACCAC CAAATGACAG AGATGCAGAC CAAGACAAAA GGAAAAAACA 1140
ACAGAAGGGA TTTTTGTCCT TGAGACGTGC TATGCAAATT CTTTTCAATT AGTTTCCTAT 1200
TAATGATTCC ATCTTGAACA TTTAGAGCTG CTCAACCCAG GCAGCATCTA CGTTTTGAAG 1260
TAGTAAGTTC TCCATTCCTA GCAGAGTCGG AGGAGAAGCT CAGCTGTTAT CCACCAGAAA 1320
TTCTATTAAA AGGATGAAAG GTTGAACTAG ATGACTTCTC ATTCTGAAGA CTGTAATTCA 1380
GCAGAACTGA CTAATCCCTG GCAAATGATA CCCTTTCTGA GTATGCATGT GTCACTGAAA 1440
GTCACTCAGA CAAACCAGAC TATTTGTAAA TAGGTCTGAT TATCTGCAAA TTAGTTGATT 1500
GAAGGTTCCC GGGTATCAAG CAGGGCTTAT TTTAAGAAAT TAAGTTAATT TAGATAATAG 1560
CTGTGTTGAA AAGCAACAAG TTCAAAAACA ATTAAAAAGA ATGCAGCTTC CCTTTTATTT 1620
TTTTCAACTC TATATTTTCT TTTCAAATTG CTTCTAATAG ACCATCTGTT AAGAAAGCCT 1680
CTTTTGACCG GGTGCAATGG CTCACACCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCAG 1740
GTGGATCACC TGAGGTCATG AGTTCAAGAT AGCCTGAGCA ACATGGTGAA ACCCCGTTTC 1800
TACTAAAAAC ACAGAAATTA GCTGGGCGTC GTGGCACGCG CCTATAAACC CAGCTACTCT 1860
GGAGGCTGAG GCACAAGAAT TGCTTGAACC CGGGAGGCAG AGGTTGCAGT GAGCTGAGAT 1920
AGCACCATTA CACTCCAGCC TGAGAGACAG AGCAAGACTC CATCTCAAAA ATAAAAAAAA 1980
GAAAGGCTCT TTCGTAAATT ACTTAAATAT GCTTAGAAGT CATTATTACT TTTTAAGTCA 2040
ATAGAAGTCT TTTTAGTTTA TCTAATAGCA TATTAATTCC TATGCTTTAT GTGTTTGTAC 2100
CCACACAACA CCCAGCCCTG CACCTAACAC ATAACAGGTG CTCAATAGAT GTTCATTGAA 2160
TAAATTGGTT GCAAAAACCG AGTGTATACA TTGAACATTT CTGCATATTG GTGATAATAA 2220
TAGTATTTTG AACACTTGTT CTATGCCAGT GACTGGGTCA AATAAACACT CAACCTCATA 2280
GTAATATCTG CGAAGTGATT GCTACATTAG CCCCATTTTA CAGATGATGC AACTGAGGCT 2340
GGTGAGAGGC AGAGCCAGGA TTCAAGGCCA GGCCTGTCCA ACTCCCGAGC CGAAGCTCTC 2400
AGCGAGGGTA TCAAACTGAA TCTGAATCCT CTTAGTTTAT CTATTTTAAA GTGCTGCATG 2460
TGGTATGTTC AGGAGACGAA AACTCTCTGA TGAGGCACGT GTGGATGGGA TGGCAGGGCT 2520
GAGAAGGCCG GCTCCCCCAC GGGGTGTGCA CAACCTACCT CCCCAGCTGT TTCTGCTACC 2580
GGCTGGGGCC TTCAACTCCA CCGCCTCCCC TCCCCCAGGC CCTAAATCAC TCTCAGGCCT 2640
TTTGTTCTTC CCCACAGCTG CTCAGCAAAT TCCTTGATTT GAAATTACGA TCACAGGTTG 2700
GAGTGCTACT TAAAATAATT TTGCCAAATG TTCCATCTCT CTGTGTTGAT GAATATAATG 2760