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

TagContent
EnhancerAtlas ID
HS074-07518 
Organism
Homo sapiens 
Tissue/cell
GM19239 
Coordinate
chr19:11205060-11207820 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr19:11205882-11205896AAGAAATGAGTCAT+7.12
JUN(var.2)MA0489.1chr19:11207063-11207077ATGACTCATTTCTT-7.12
JUN(var.2)MA0489.1chr19:11207058-11207072AGGAAATGACTCAT+8.12
JUN(var.2)MA0489.1chr19:11205887-11205901ATGAGTCATTTCCT-8.12
SREBF1MA0595.1chr19:11205756-11205766GTGGGGTGAT-6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_01022chr19:11206333-11207663Adrenal_Gland
SE_12085chr19:11204949-11207773CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11204971-11207608CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11204867-11207840CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11204855-11208057CD8_primiary
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_23239chr19:11206100-11207601Colon_Crypt_1
SE_24095chr19:11204989-11205979Colon_Crypt_2
SE_24095chr19:11206366-11207012Colon_Crypt_2
SE_24095chr19:11207130-11207564Colon_Crypt_2
SE_24928chr19:11205061-11206082Colon_Crypt_3
SE_24928chr19:11206201-11206876Colon_Crypt_3
SE_26902chr19:11204916-11207828Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11204956-11208148Fetal_Muscle
SE_31737chr19:11204927-11207763Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11204941-11207563HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11205013-11206118NHDF-Ad
SE_44493chr19:11206328-11207705NHDF-Ad
SE_44932chr19:11205113-11207883NHLF
SE_47693chr19:11204994-11205972Pancreas
SE_47693chr19:11206368-11206786Pancreas
SE_47693chr19:11207237-11207566Pancreas
SE_49361chr19:11205119-11206191Right_Atrium
SE_49361chr19:11206197-11207709Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11205007-11205595VACO_503
SE_64571chr19:11204940-11207695NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
SE_68998chr19:11207123-11207544H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr191120695311207150
chr191120569611206011
chr191120634811207740
Enhancer Sequence
TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTATAGGC GTGAGCCCCC GAACCCGGCC 60
ACTCCCAGCT AAGTTTAAAT TTTTTGTTTG TTTGTTCGTT TGTTTTTATT TTTTGAGACA 120
GAGTCTCCCG CCCAGGCTGG AGCGCAGATC ACTGCATCCT TGACCTCCCA GGCTTAAGCC 180
ATCCTCCCCA CTCAGCCTCC CAAGTAGCTG GGATTACAGG TGTGTGCCAC TATGCTTGGC 240
TAAGTTGTGT ATTTTTTGTA GAGATGGGGT TCAAGGGATT CTCGCTTTGT TGCCTCGGTT 300
GGTCTCAAAC TCCTGGGCTC AAGCAGTCCT CCCTCCTCAG CCTCCCAAGG TGCTGGGGAA 360
ATCCACTTTT GAAACATTGT CTGGAGAGTT GCCCAGGTGG TAGATCACAG AAATAGGTCA 420
TCGTGGGGTC CTTCCCATGG GTGCAGTCTT GAGCCACCTG TGGCCAGCAA ATATTTGGAG 480
AATAATAGTC AGGGGAGAGC TTGAGGTCCA GGGAAAGGTT TTGTTTTTCT TCAGGGAAAG 540
GTTTTTATTG TTCTTTATCC CTCCTTAAAG GACCTTCAGG TGTTACTGAC ATTCCCGGTC 600
TACCCAGTGG CACATTTAGT TTGTAAGCTG GGCCCTCGTA CAGAGGTAGG GAGGTGAGAG 660
CATTGGATTA GTGGTCACCA AAGCTGCGGT CACCTAGTGG GGTGATCAGA GGCTCCTCCC 720
TTAAGATCTT GATTGCCAAC GCCTCTGGCC CAACTTTCCT TTTTATTTAT CGCAAGCCTC 780
CTGGAATCTC AATTGCTTTT TGCCCACCCG GTGTGTCAGC ACAAGAAATG AGTCATTTCC 840
TCCTTTAAGC ACAGTTGAAA TTGAGCTGTG AGTCAGTGAG GTGTGTACGA TATTGTCAAA 900
GCGGGGTGTG TACAGTATTG ACAGATCTGT AGTTGGGCAA GAGAATTATC AGAGTTTGTG 960
ACCACAGCAG ATTCCAAAGC TCGACTCATT TTCTTCTCTC TTCCTTCCCT TTTTTCTTTT 1020
CTTTTTTTTT TTTTTTTTGA CAGAGTCTCG CTCTGTTGCC CAGGCTGGAG TGCAGTGGCA 1080
CAATCTGGGC TCACTGCAGC CCCTGCCTCC TGGGTTCAAA TGATTCTCAT GTTTCAGCCT 1140
CCCGAGTAGC TGCAATTACA GGCATTCGGG TTCAAGTGAT TCTCCTGCCT CAGCCACCTG 1200
AGCAGCTGGG ATTACAGGCG CCCGCCACCA CGCCCGGCTA ATTTTTGTAT TTTTAGTAGA 1260
GACGGGGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGAACTCAG GTGATCCGCC 1320
CACTTCGGCC TCCCAAAGTG CTGAGATTAC AGACGTGAGT CACCGCGCCC AGCCTGTTCT 1380
GTTCTTTAAT TCTCAAAACA CCCTCTAGGA AGTAGAGACT GCCATTCTCC CCCATTTTAC 1440
AGATCAGGAA ACTGAGTCCC AGAAGGATTT AGTCAGTTAC CCAAGTTGTT CTAGTTAAAT 1500
GGCCTGGAAA GCCAGTGAAG CCCAGGATTG TCTATCTAAC CCCCTTACTA CTCTAACTTT 1560
CAGGGAATCC ACATGAATGT GCTGGGTCAA CCATCAAAGT TGAAATGGAT AAAGGGGGCT 1620
GGATGCGGTG GCTGATGCCT GTAATCCTAG CACTTTGGGA GGCCGAGATG GGTGGGTGGA 1680
TTGCTTGAGC CCAAGAGTTT GAGACCAGCC TGGGCAACAT AGTGAGACAC CTGTCTCTGC 1740
AAAAAATAAA TAAAAAGTTA GCTGAGTGTG ATGGTGCACC CCTCTAGTCA CAGCTGTTGA 1800
GTTAGGCTTA GGCAGGAGGA TCGCATGAAC CTGGGAGGTG GAGGCGGCCG TGAGCCTCAG 1860
TCATGCCACT GCACTCCAAC CTGGGCAACA GAGTGAAAGC CGGTGTCCGA AAGAGAAAGA 1920
AAAAAAGACA TAGATACATC TTTTAAAGTT AGGTTGTATG TTAATTACCT ACAACTCAGT 1980
TTCAACTGTG CTTAAAGGAG GAAATGACTC ATTTCTTGCT ACATATCAAA TTAGCCCAAA 2040
ATGTAGTGGC TTAAAACAAC ACATTTATGA TTTCTCAGTT TTTGCGTGTC AGGAATTTGG 2100
AAGCAGCACA GCTAGACGGT TCCAGCTCAG GGTCTCTCAT GAAGTTGCAA TCAAAATATT 2160
GGCAGGAGAG AAAAACATAT TTTCAGAAGC TGCAGGCATA GGAAGACTTG GCTGGGGTTG 2220
AAGGATCCAC TTCCAAGATG GCGCACTCAG TGGCTCTTGG CTGGAGGCCT CAGTTCCCTG 2280
CTGCGTGGAG CTCTCCCTCC AGCTGCTTGA GTGGACTCAT GACATGCAGC TGGCCTCCCC 2340
TGGAGCAGTC GATCCAACAA TGAGCATGGC CATGAACTAG GCTCAGAAGC CACTCCCTGT 2400
CGTCTCTACA TTTTCCTATC AGAAGCAAGT CATTAAAAGT CCAGTGCCAC TCCAGGGGAG 2460
ACGAATTAGG CTCTGCCTTC TGAAAGGATT ATCACAGAAG ATGCGGTCCT ATATTCTTTT 2520
TTTAAAATTA TTCTTTTTTT TATTTTGTAG AGATGGGGTC TTGGTATGTT GCCTAGGCCA 2580
GTCTGGAATT CCTGGGCTCA AACAATCCTG TCTCTGCCTC CCAAAGTGTT GGGATTACAG 2640
GCATGAGCCA CTGCACCTGG TCATGTGGTC ATATTTTCTT TTTCTTTTTT TTTTTTTTTT 2700
GAGACAGAGT CTCTGTCGCC CAGGCTGGAG TATGGTGGCG TGATCTCAGT TCACTGCAGC 2760