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

TagContent
EnhancerAtlas ID
HS138-03895 
Organism
Homo sapiens 
Tissue/cell
MSC_BM 
Coordinate
chr1:235090390-235093080 
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
AACCCCATTT GATGCTCCTG ATGAGGTCCG TGAGGTCCGA GACCCCTGCA TGAACCAGTC 60
AGATCACCAT GGAACAAGTC GCCCCAGGGC ATGGCTGTCT CCAGCCGCTC TGAGTAGCCA 120
GCGGTGCAGC CAGCTGGTCT CAGATTTGGG CTGTGATGAG TCTGGATGGC AGAAGAACAA 180
GAGGGATGGG AAATTGAGGG AGGGCCTCAT TGAAAGGGCT CACTCCAGGA GCCAGAAAAC 240
CAGAAGAGCC TAAGGGACCC AGAGCTAGAG TGAGACCAGA GATGCACAGT CCCCATGAGG 300
ACAAAGAGCC CAGTGAGGAG AAAGGGAGAG GTAAAAGGAT AAAAGAGTCA GAAGGAGTTT 360
CAGAATCTAA GAGCTCCAAA AATAAACCTT TCCCTTTGTA TCACTTTTCT CTTTTTACTT 420
TAGTTGCTCT CAACTTGCTG CTTCCTTTTT TTAAAAATTC TAGCAATTCT GCAGGAAACC 480
AGAAGTGTGA ACCAAACACA GTAACTCTAG GTGTTATGGC GCTGTCCTGC TCACCCTTCT 540
TTTGGCCTAC TGGCTTCAAA GGTAGGCACA CACACCGTCC CTTTTCTAAT GATCCGGTCG 600
TGGATTCAGG CTCAGTAAGC CAAGACCACA AGCAACAGGG CTTGGGCTCC ATCTGCCTCG 660
GCTGCTTGCA GCTGCCTTCC AGGAAGTGCT GGAACAGCAG AAGCAGCTAG CAGTGCGCTC 720
AAGAAGTGGT CAGCAGTTGG GAGCAGCTGG AGGAGGGGAG GCCAGTGAGC AAGTATCAGC 780
TTGGGAAATA GGGTTTCGGC TGAACAAAGT TCACTGCTGT TTTCTGAGAA AGCAGAACCT 840
AGTGGAGCCA CCCTAGAGAA TAAGGAGAGG AGCAACTGGA ACTGAGTGTT GGCTCCAAAC 900
TTCCACGGCA TGATATGCTT GGCCACCCAA TTGTGATCAG GGCCATTGTT GTTCCCCTGG 960
GGGCAGGGGG CAGAGGGCAG GCCGCCGCTC GGAGTAAAAA GGGAAGACAG ACAGGCAGTC 1020
CAAACACCAC CAAATGACAG AGATGCAGAC CAAGACAAAA GGAAAAAACA ACAGAAGGGA 1080
TTTTTGTCCT TGAGACGTGC TATGCAAATT CTTTTCAATT AGTTTCCTAT TAATGATTCC 1140
ATCTTGAACA TTTAGAGCTG CTCAACCCAG GCAGCATCTA CGTTTTGAAG TAGTAAGTTC 1200
TCCATTCCTA GCAGAGTCGG AGGAGAAGCT CAGCTGTTAT CCACCAGAAA TTCTATTAAA 1260
AGGATGAAAG GTTGAACTAG ATGACTTCTC ATTCTGAAGA CTGTAATTCA GCAGAACTGA 1320
CTAATCCCTG GCAAATGATA CCCTTTCTGA GTATGCATGT GTCACTGAAA GTCACTCAGA 1380
CAAACCAGAC TATTTGTAAA TAGGTCTGAT TATCTGCAAA TTAGTTGATT GAAGGTTCCC 1440
GGGTATCAAG CAGGGCTTAT TTTAAGAAAT TAAGTTAATT TAGATAATAG CTGTGTTGAA 1500
AAGCAACAAG TTCAAAAACA ATTAAAAAGA ATGCAGCTTC CCTTTTATTT TTTTCAACTC 1560
TATATTTTCT TTTCAAATTG CTTCTAATAG ACCATCTGTT AAGAAAGCCT CTTTTGACCG 1620
GGTGCAATGG CTCACACCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCAG GTGGATCACC 1680
TGAGGTCATG AGTTCAAGAT AGCCTGAGCA ACATGGTGAA ACCCCGTTTC TACTAAAAAC 1740
ACAGAAATTA GCTGGGCGTC GTGGCACGCG CCTATAAACC CAGCTACTCT GGAGGCTGAG 1800
GCACAAGAAT TGCTTGAACC CGGGAGGCAG AGGTTGCAGT GAGCTGAGAT AGCACCATTA 1860
CACTCCAGCC TGAGAGACAG AGCAAGACTC CATCTCAAAA ATAAAAAAAA GAAAGGCTCT 1920
TTCGTAAATT ACTTAAATAT GCTTAGAAGT CATTATTACT TTTTAAGTCA ATAGAAGTCT 1980
TTTTAGTTTA TCTAATAGCA TATTAATTCC TATGCTTTAT GTGTTTGTAC CCACACAACA 2040
CCCAGCCCTG CACCTAACAC ATAACAGGTG CTCAATAGAT GTTCATTGAA TAAATTGGTT 2100
GCAAAAACCG AGTGTATACA TTGAACATTT CTGCATATTG GTGATAATAA TAGTATTTTG 2160
AACACTTGTT CTATGCCAGT GACTGGGTCA AATAAACACT CAACCTCATA GTAATATCTG 2220
CGAAGTGATT GCTACATTAG CCCCATTTTA CAGATGATGC AACTGAGGCT GGTGAGAGGC 2280
AGAGCCAGGA TTCAAGGCCA GGCCTGTCCA ACTCCCGAGC CGAAGCTCTC AGCGAGGGTA 2340
TCAAACTGAA TCTGAATCCT CTTAGTTTAT CTATTTTAAA GTGCTGCATG TGGTATGTTC 2400
AGGAGACGAA AACTCTCTGA TGAGGCACGT GTGGATGGGA TGGCAGGGCT GAGAAGGCCG 2460
GCTCCCCCAC GGGGTGTGCA CAACCTACCT CCCCAGCTGT TTCTGCTACC GGCTGGGGCC 2520
TTCAACTCCA CCGCCTCCCC TCCCCCAGGC CCTAAATCAC TCTCAGGCCT TTTGTTCTTC 2580
CCCACAGCTG CTCAGCAAAT TCCTTGATTT GAAATTACGA TCACAGGTTG GAGTGCTACT 2640
TAAAATAATT TTGCCAAATG TTCCATCTCT CTGTGTTGAT GAATATAATG 2690